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 4:154589513 (forward strand) | View in location tab

Co-located

with COSMIC COSM218791 (C/T) ; HGMD-PUBLIC CM810009

Most severe consequence
Clinical significance

Synonyms

LSDB 1926

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

4:g.154589513C>T
ENST00000302053.5:c.104G>A
ENSP00000306361.3:p.Arg35His
ENST00000403106.5:c.104G>A
ENSP00000385981.3:p.Arg35His
ENST00000622532.1:c.104G>A
ENSP00000478487.1:p.Arg35His
LRG_557:g.6233G>A
LRG_557t2.1:c.104G>A
LRG_557p2.1:p.Arg35His
LRG_557t1.1:c.104G>A
LRG_557p1.1:p.Arg35His

Variation displays