Canonical Allele Identifier: CA2129379101
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.36384991A= , CM000676.2:g.36384991A= GRCh38
NC_000014.8:g.36854196A= , CM000676.1:g.36854196A= GRCh37
NC_000014.7:g.35923947A= NCBI36

Transcript Alleles

HGVS Amino-acid change
XM_011537428.1:c.319-12168A= XP_011535730.1:n.319-12168A=
XR_943756.1:n.358+23895A=