Canonical Allele Identifier: CA1207463725
Gene:

Linked Data

dbSNP Id: rs1660425008

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.172741771T>A , CM000663.2:g.172741771T>A GRCh38
NC_000001.10:g.172710911T>A , CM000663.1:g.172710911T>A GRCh37
NC_000001.9:g.170977534T>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_922289.1:n.27-34048T>A