Canonical Allele Identifier: CA2129379046
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.36384836C= , CM000676.2:g.36384836C= GRCh38
NC_000014.8:g.36854041C= , CM000676.1:g.36854041C= GRCh37
NC_000014.7:g.35923792C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XM_011537428.1:c.319-12323C= XP_011535730.1:n.319-12323C=
XR_943756.1:n.358+23740C=