Canonical Allele Identifier: CA82198663
Gene:

Linked Data

dbSNP Id: rs1676232

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.117515992G>A , CM000665.2:g.117515992G>A GRCh38
NC_000003.11:g.117234839G>A , CM000665.1:g.117234839G>A GRCh37
NC_000003.10:g.118717529G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_924361.1:n.298+1492G>A
XR_001740490.2:n.4763+1492G>A
XR_924361.2:n.127+1492G>A