Canonical Allele Identifier: CA2170931670
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.38614896T= , CM000677.2:g.38614896T= GRCh38
NC_000015.9:g.38907097T= , CM000677.1:g.38907097T= GRCh37
NC_000015.8:g.36694389T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_001751736.1:n.281+2441T=