Canonical Allele Identifier: CA2072411480
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.131529567C= , CM000674.2:g.131529567C= GRCh38
NC_000012.11:g.132014112C= , CM000674.1:g.132014112C= GRCh37
NC_000012.10:g.130580065C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_945564.1:n.1076+208G=
XR_001749407.2:n.1067+208G=