Canonical Allele Identifier: CA529297685
Gene:

Linked Data

dbSNP Id: rs1340354646

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.220491635T>A , CM000663.2:g.220491635T>A GRCh38
NC_000001.10:g.220664977T>A , CM000663.1:g.220664977T>A GRCh37
NC_000001.9:g.218731600T>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_922615.1:n.256-599T>A
XR_001737822.1:n.557-599T>A