Original source

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

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

Chromosome 4:154589505 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM010045

Most severe consequence
Clinical significance

Synonyms

LSDB 1929

This variation has 12 HGVS names - click the plus to show

4:g.154589505T>C
ENST00000302053.5:c.112A>G
ENSP00000306361.3:p.Arg38Gly
ENST00000403106.5:c.112A>G
ENSP00000385981.3:p.Arg38Gly
ENST00000622532.1:c.112A>G
ENSP00000478487.1:p.Arg38Gly
LRG_557:g.6241A>G
LRG_557t1.1:c.112A>G
LRG_557p1.1:p.Arg38Gly
LRG_557t2.1:c.112A>G
LRG_557p2.1:p.Arg38Gly

Variation displays