Canonical Allele Identifier: CA1689218086
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.13400569T= , CM000669.2:g.13400569T= GRCh38
NC_000007.13:g.13440194T= , CM000669.1:g.13440194T= GRCh37
NC_000007.12:g.13406719T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_001745097.1:n.147+90246T=