Canonical Allele Identifier: CA1374121531
Gene:

Linked Data

dbSNP Id: rs1428169809

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.72266722C>A , CM000665.2:g.72266722C>A GRCh38
NC_000003.11:g.72315873C>A , CM000665.1:g.72315873C>A GRCh37
NC_000003.10:g.72398563C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_940958.1:n.835+8386G>T