Canonical Allele Identifier: CA2137107139
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.52417665T= , CM000676.2:g.52417665T= GRCh38
NC_000014.8:g.52884383T= , CM000676.1:g.52884383T= GRCh37
NC_000014.7:g.51954133T= NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_943866.1:n.3038A=