Original source

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

Alleles
C/T | Ancestral: C | Ambiguity code: Y
Location

Chromosome 2:233767873 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM931136

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB 2010_April_001_128_UGT1A1_191740_0004, 5990

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

2:g.233767873C>T
ENST00000373445.1:c.1012C>T
ENSP00000362544.1:p.Arg338Ter
ENST00000373409.4:c.1024C>T
ENSP00000362508.3:p.Arg342Ter
ENST00000305139.7:c.1018C>T
ENSP00000303174.6:p.Arg340Ter
ENST00000482026.2:c.1024C>T
ENSP00000418532.1:p.Arg342Ter
ENST00000446481.3:c.217C>T
ENSP00000401541.1:p.Arg73Ter
ENST00000373424.2:c.217C>T
ENSP00000362523.1:p.Arg73Ter
ENST00000373426.3:c.1012C>T
ENSP00000362525.3:p.Arg338Ter
ENST00000450233.1:c.1024C>T
ENSP00000408608.1:p.Arg342Ter
ENST00000360418.4:c.1021C>T
ENSP00000353593.3:p.Arg341Ter
ENST00000609767.2:c.1024C>T
ENSP00000476805.2:p.Arg342Ter
ENST00000373414.3:c.1024C>T
ENSP00000362513.3:p.Arg342Ter
ENST00000305208.6:c.1021C>T
ENSP00000304845.5:p.Arg341Ter
ENST00000406651.1:c.217C>T
ENSP00000386107.1:p.Arg73Ter
ENST00000344644.6:c.1012C>T
ENSP00000343838.5:p.Arg338Ter
ENST00000373450.4:c.1012C>T
ENSP00000362549.4:p.Arg338Ter
ENST00000354728.4:c.1012C>T
ENSP00000346768.4:p.Arg338Ter
LRG_733:g.12601C>T
LRG_733t1.1:c.1021C>T
LRG_733p1.1:p.Arg341Ter

Variation displays