Original source

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

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

Chromosome 19:40395495 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM011006

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB 13365, 2010_April_001_087_PRX_605725_0001

This variation has 8 HGVS names - click the plus to show

19:g.40395495G>A
ENST00000291825.8:c.*3062C>T
ENST00000324001.7:c.2857C>T
ENSP00000326018.6:p.Arg953Ter
LRG_265:g.22870C>T
LRG_265t2.1:c.2857C>T
LRG_265p2.1:p.Arg953Ter
LRG_265t1.1:c.*3062C>T

Variation displays