Canonical Allele Identifier: CA200491664
Gene:

Linked Data

dbSNP Id: rs61110367

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.129576798C>A , CM000671.2:g.129576798C>A GRCh38
NC_000009.11:g.132339077C>A , CM000671.1:g.132339077C>A GRCh37
NC_000009.10:g.131378898C>A NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_930390.1:n.182+1200C>A