Canonical Allele Identifier: CA1817437259
Gene:

Linked Data

dbSNP Id: rs1815191592

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.125474124G>A , CM000670.2:g.125474124G>A GRCh38
NC_000008.10:g.126486366G>A , CM000670.1:g.126486366G>A GRCh37
NC_000008.9:g.126555548G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_928628.1:n.256+810G>A