Canonical Allele Identifier: CA2485976211
Gene:

Linked Data

dbSNP Id: rs1658287693

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.213682276T>A , CM000663.2:g.213682276T>A GRCh38
NC_000001.10:g.213855619T>A , CM000663.1:g.213855619T>A GRCh37
NC_000001.9:g.211922242T>A NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_001738463.1:n.601-49141T>A
XR_001738464.1:n.426-49141T>A