Canonical Allele Identifier: CA2047190483
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.76004925C= , CM000674.2:g.76004925C= GRCh38
NC_000012.11:g.76398705C= , CM000674.1:g.76398705C= GRCh37
NC_000012.10:g.74684972C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_945110.1:n.311+1264G=
XR_001749218.2:n.402+1264G=
XR_945110.3:n.402+1264G=