Canonical Allele Identifier: CA1728106760
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.97388546C= , CM000669.2:g.97388546C= GRCh38
NC_000007.13:g.97017858C= , CM000669.1:g.97017858C= GRCh37
NC_000007.12:g.96855794C= NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_001745293.1:n.127-59899G=