Canonical Allele Identifier: CA1947280410
Gene:

Linked Data

dbSNP Id: rs1171145725

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.746930G>A , CM000673.2:g.746930G>A GRCh38
NC_000011.9:g.746930G>A , CM000673.1:g.746930G>A GRCh37
NC_000011.8:g.736930G>A NCBI36
NG_008160.1:g.4499G>A

Transcript Alleles

HGVS Amino-acid change
XR_930962.1:n.340G>A
XR_930963.1:n.259+81G>A
XR_930962.2:n.2432G>A