Canonical Allele Identifier: CA2129379032
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.36384796G= , CM000676.2:g.36384796G= GRCh38
NC_000014.8:g.36854001G= , CM000676.1:g.36854001G= GRCh37
NC_000014.7:g.35923752G= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XM_011537428.1:c.319-12363G= XP_011535730.1:n.319-12363G=
XR_943756.1:n.358+23700G=