Canonical Allele Identifier: CA2129379114
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.36385033A= , CM000676.2:g.36385033A= GRCh38
NC_000014.8:g.36854238A= , CM000676.1:g.36854238A= GRCh37
NC_000014.7:g.35923989A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XM_011537428.1:c.319-12126A= XP_011535730.1:n.319-12126A=
XR_943756.1:n.358+23937A=