Canonical Allele Identifier: CA1695606399
Gene:

Linked Data

dbSNP Id: rs1783618760

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.25831435C>T , CM000669.2:g.25831435C>T GRCh38
NC_000007.13:g.25871055C>T , CM000669.1:g.25871055C>T GRCh37
NC_000007.12:g.25837580C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_108752.3:n.472G>A
XR_927108.1:n.446G>A
XR_927109.1:n.528G>A
XR_927110.1:n.432G>A
XR_108752.4:n.486G>A
XR_927110.2:n.611G>A