Canonical Allele Identifier: CA2129379089
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.36384954C= , CM000676.2:g.36384954C= GRCh38
NC_000014.8:g.36854159C= , CM000676.1:g.36854159C= GRCh37
NC_000014.7:g.35923910C= NCBI36

Transcript Alleles

HGVS Amino-acid change
XM_011537428.1:c.319-12205C= XP_011535730.1:n.319-12205C=
XR_943756.1:n.358+23858C=