Canonical Allele Identifier: CA2485976238
Gene:

Linked Data

dbSNP Id: rs1571659483

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.213682344T>A , CM000663.2:g.213682344T>A GRCh38
NC_000001.10:g.213855687T>A , CM000663.1:g.213855687T>A GRCh37
NC_000001.9:g.211922310T>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_001738463.1:n.601-49073T>A
XR_001738464.1:n.426-49073T>A