Canonical Allele Identifier: CA663648620
Gene:

Linked Data

dbSNP Id: rs1190173534

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.30201898G>A , CM000672.2:g.30201898G>A GRCh38
NC_000010.10:g.30490827G>A , CM000672.1:g.30490827G>A GRCh37
NC_000010.9:g.30530833G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_930791.1:n.1193-1589G>A
XR_930791.2:n.1449-1589G>A