Canonical Allele Identifier: CA13088858
Gene:

Linked Data

dbSNP Id: rs13294895

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.108074895C>T , CM000671.2:g.108074895C>T GRCh38
NC_000009.11:g.110837176C>T , CM000671.1:g.110837176C>T GRCh37
NC_000009.10:g.109876997C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_930239.1:n.461-21601G>A
XR_001746881.1:n.668-21601G>A
XR_001746882.1:n.668-21601G>A