Canonical Allele Identifier: CA2137107022
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.52417565A= , CM000676.2:g.52417565A= GRCh38
NC_000014.8:g.52884283A= , CM000676.1:g.52884283A= GRCh37
NC_000014.7:g.51954033A= NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_943866.1:n.3138T=