Canonical Allele Identifier: CA1728106670
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.97388344C= , CM000669.2:g.97388344C= GRCh38
NC_000007.13:g.97017656C= , CM000669.1:g.97017656C= GRCh37
NC_000007.12:g.96855592C= NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_001745293.1:n.127-59697G=