Canonical Allele Identifier: CA13108512
Gene:

Linked Data

dbSNP Id: rs11789399

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.118597008G>A , CM000671.2:g.118597008G>A GRCh38
NC_000009.11:g.121359286G>A , CM000671.1:g.121359286G>A GRCh37
NC_000009.10:g.120399107G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_930297.1:n.32+133C>T
XR_930297.2:n.32+133C>T