Canonical Allele Identifier: CA200491628
Gene:

Linked Data

dbSNP Id: rs1043273771

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.129576770G>A , CM000671.2:g.129576770G>A GRCh38
NC_000009.11:g.132339049G>A , CM000671.1:g.132339049G>A GRCh37
NC_000009.10:g.131378870G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_930390.1:n.182+1172G>A