Canonical Allele Identifier: CA185688655
Gene:

Linked Data

dbSNP Id: rs928232080

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.126999469G>A , CM000670.2:g.126999469G>A GRCh38
NC_000008.10:g.128011714G>A , CM000670.1:g.128011714G>A GRCh37
NC_000008.9:g.128080896G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_001746076.2:n.1301-7086G>A