Canonical Allele Identifier: CA1728106682
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.97388374C= , CM000669.2:g.97388374C= GRCh38
NC_000007.13:g.97017686C= , CM000669.1:g.97017686C= GRCh37
NC_000007.12:g.96855622C= NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_001745293.1:n.127-59727G=