Canonical Allele Identifier: CA199632576
Gene:

Linked Data

dbSNP Id: rs10984561

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.119496299C>A , CM000671.2:g.119496299C>A GRCh38
NC_000009.11:g.122258577C>A , CM000671.1:g.122258577C>A GRCh37
NC_000009.10:g.121298398C>A NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_930304.1:n.161+27596G>T
XR_930305.1:n.161+27596G>T
XR_930304.2:n.188+27596G>T
XR_930305.2:n.188+27596G>T