Canonical Allele Identifier: CA2137106998
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.52417539C= , CM000676.2:g.52417539C= GRCh38
NC_000014.8:g.52884257C= , CM000676.1:g.52884257C= GRCh37
NC_000014.7:g.51954007C= NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_943866.1:n.3164G=