Canonical Allele Identifier: CA185688672
Gene:

Linked Data

dbSNP Id: rs144990965

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.126999545G>A , CM000670.2:g.126999545G>A GRCh38
NC_000008.10:g.128011790G>A , CM000670.1:g.128011790G>A GRCh37
NC_000008.9:g.128080972G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_001746076.2:n.1301-7010G>A