Canonical Allele Identifier: CA2072411525
Gene:

Linked Data

dbSNP Id: rs1953652776

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.131529666C>T , CM000674.2:g.131529666C>T GRCh38
NC_000012.11:g.132014211C>T , CM000674.1:g.132014211C>T GRCh37
NC_000012.10:g.130580164C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_945564.1:n.1076+109G>A
XR_001749407.2:n.1067+109G>A