Canonical Allele Identifier: CA255087103
Gene:

Linked Data

dbSNP Id: rs1056159601

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.94853099G>A , CM000675.2:g.94853099G>A GRCh38
NC_000013.10:g.95505353G>A , CM000675.1:g.95505353G>A GRCh37
NC_000013.9:g.94303354G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_110754.1:n.257-52365G>A