Canonical Allele Identifier: CA2072411536
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.131529677C= , CM000674.2:g.131529677C= GRCh38
NC_000012.11:g.132014222C= , CM000674.1:g.132014222C= GRCh37
NC_000012.10:g.130580175C= NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_945564.1:n.1076+98G=
XR_001749407.2:n.1067+98G=