Canonical Allele Identifier: CA2129379079
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.36384940A= , CM000676.2:g.36384940A= GRCh38
NC_000014.8:g.36854145A= , CM000676.1:g.36854145A= GRCh37
NC_000014.7:g.35923896A= NCBI36

Transcript Alleles

HGVS Amino-acid change
XM_011537428.1:c.319-12219A= XP_011535730.1:n.319-12219A=
XR_943756.1:n.358+23844A=