Canonical Allele Identifier: CA2129379069
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.36384915A= , CM000676.2:g.36384915A= GRCh38
NC_000014.8:g.36854120A= , CM000676.1:g.36854120A= GRCh37
NC_000014.7:g.35923871A= NCBI36

Transcript Alleles

HGVS Amino-acid change
XM_011537428.1:c.319-12244A= XP_011535730.1:n.319-12244A=
XR_943756.1:n.358+23819A=