Canonical Allele Identifier: CA2137107048
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.52417584T= , CM000676.2:g.52417584T= GRCh38
NC_000014.8:g.52884302T= , CM000676.1:g.52884302T= GRCh37
NC_000014.7:g.51954052T= NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_943866.1:n.3119A=