Canonical Allele Identifier: CA2129379034
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.36384798A= , CM000676.2:g.36384798A= GRCh38
NC_000014.8:g.36854003A= , CM000676.1:g.36854003A= GRCh37
NC_000014.7:g.35923754A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XM_011537428.1:c.319-12361A= XP_011535730.1:n.319-12361A=
XR_943756.1:n.358+23702A=