Canonical Allele Identifier: CA2072411495
Gene:

Linked Data

dbSNP Id: rs1953652186

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.131529601G>A , CM000674.2:g.131529601G>A GRCh38
NC_000012.11:g.132014146G>A , CM000674.1:g.132014146G>A GRCh37
NC_000012.10:g.130580099G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_945564.1:n.1076+174C>T
XR_001749407.2:n.1067+174C>T