Original source

Variants (including SNPs and indels) imported from dbSNP (mapped to GRCh38) (release 138) | View in dbSNP

Alleles
A/G | Ancestral: A | Ambiguity code: R
Location

Chromosome 2:233767922 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM941353

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB 2010_April_001_133_UGT1A1_191740_0019, 6005

This variation has 36 HGVS names - click the plus to show

2:g.233767922A>G
ENST00000373445.1:c.1061A>G
ENSP00000362544.1:p.Gln354Arg
ENST00000305139.7:c.1067A>G
ENSP00000303174.6:p.Gln356Arg
ENST00000373409.4:c.1073A>G
ENSP00000362508.3:p.Gln358Arg
ENST00000482026.2:c.1073A>G
ENSP00000418532.1:p.Gln358Arg
ENST00000446481.3:c.266A>G
ENSP00000401541.1:p.Gln89Arg
ENST00000373424.2:c.266A>G
ENSP00000362523.1:p.Gln89Arg
ENST00000373426.3:c.1061A>G
ENSP00000362525.3:p.Gln354Arg
ENST00000450233.1:c.1073A>G
ENSP00000408608.1:p.Gln358Arg
ENST00000360418.4:c.1070A>G
ENSP00000353593.3:p.Gln357Arg
ENST00000609767.2:c.1073A>G
ENSP00000476805.2:p.Gln358Arg
ENST00000373414.3:c.1073A>G
ENSP00000362513.3:p.Gln358Arg
ENST00000406651.1:c.266A>G
ENSP00000386107.1:p.Gln89Arg
ENST00000305208.6:c.1070A>G
ENSP00000304845.5:p.Gln357Arg
ENST00000344644.6:c.1061A>G
ENSP00000343838.5:p.Gln354Arg
ENST00000373450.4:c.1061A>G
ENSP00000362549.4:p.Gln354Arg
ENST00000354728.4:c.1061A>G
ENSP00000346768.4:p.Gln354Arg
LRG_733:g.12650A>G
LRG_733t1.1:c.1070A>G
LRG_733p1.1:p.Gln357Arg

Variation displays