Canonical Allele Identifier: CA663648597
Gene:

Linked Data

dbSNP Id: rs1313410101

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.30201857G>A , CM000672.2:g.30201857G>A GRCh38
NC_000010.10:g.30490786G>A , CM000672.1:g.30490786G>A GRCh37
NC_000010.9:g.30530792G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_930791.1:n.1193-1630G>A
XR_930791.2:n.1449-1630G>A