Canonical Allele Identifier: CA1715429591
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.69146883C= , CM000669.2:g.69146883C= GRCh38
NC_000007.13:g.68611870C= , CM000669.1:g.68611870C= GRCh37
NC_000007.12:g.68249806C= NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_927647.1:n.88-757G=