Canonical Allele Identifier: CA2137107135
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.52417663C= , CM000676.2:g.52417663C= GRCh38
NC_000014.8:g.52884381C= , CM000676.1:g.52884381C= GRCh37
NC_000014.7:g.51954131C= NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_943866.1:n.3040G=