Canonical Allele Identifier: CA2072411522
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.131529661A= , CM000674.2:g.131529661A= GRCh38
NC_000012.11:g.132014206A= , CM000674.1:g.132014206A= GRCh37
NC_000012.10:g.130580159A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_945564.1:n.1076+114T=
XR_001749407.2:n.1067+114T=