Canonical Allele Identifier: CA2072411527
Gene:

Linked Data

dbSNP Id: rs1953652797

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.131529667C>A , CM000674.2:g.131529667C>A GRCh38
NC_000012.11:g.132014212C>A , CM000674.1:g.132014212C>A GRCh37
NC_000012.10:g.130580165C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_945564.1:n.1076+108G>T
XR_001749407.2:n.1067+108G>T