Canonical Allele Identifier: CA199632578
Gene:

Linked Data

dbSNP Id: rs10984561

Genomic Alleles

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

Transcript Alleles

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