Canonical Allele Identifier: CA1715429908
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.69147064C= , CM000669.2:g.69147064C= GRCh38
NC_000007.13:g.68612051C= , CM000669.1:g.68612051C= GRCh37
NC_000007.12:g.68249987C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_927647.1:n.88-938G=