Canonical Allele Identifier: CA1715429650
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.69146928T= , CM000669.2:g.69146928T= GRCh38
NC_000007.13:g.68611915T= , CM000669.1:g.68611915T= GRCh37
NC_000007.12:g.68249851T= NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_927647.1:n.88-802A=