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 13:102866687 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM940376

Most severe consequence
Clinical significance

Synonyms

LSDB 1779

This variation has 13 HGVS names - click the plus to show

13:g.102866687C>T
ENST00000602836.1:c.3651C>T
ENSP00000473384.1:p.Ala1218Val
ENST00000355739.6:c.2375C>T
ENSP00000347978.4:p.Ala792Val
ENST00000481099.1:n.495C>T
ENST00000610537.2:c.2375C>T
ENSP00000478667.1:p.Ala792Val
ENST00000375954.1:c.74C>T
ENSP00000365121.1:p.Ala25Val
LRG_464:g.25864C>T
LRG_464t1:c.2375C>T
LRG_464p1:p.Asp798Tyr

Variation displays