Canonical Allele Identifier: CA2137107137
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.52417664T= , CM000676.2:g.52417664T= GRCh38
NC_000014.8:g.52884382T= , CM000676.1:g.52884382T= GRCh37
NC_000014.7:g.51954132T= NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_943866.1:n.3039A=