Canonical Allele Identifier: CA2072411549
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.131529691C= , CM000674.2:g.131529691C= GRCh38
NC_000012.11:g.132014236C= , CM000674.1:g.132014236C= GRCh37
NC_000012.10:g.130580189C= NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_945564.1:n.1076+84G=
XR_001749407.2:n.1067+84G=