Canonical Allele Identifier: CA2129379047
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.36384846T= , CM000676.2:g.36384846T= GRCh38
NC_000014.8:g.36854051T= , CM000676.1:g.36854051T= GRCh37
NC_000014.7:g.35923802T= NCBI36

Transcript Alleles

HGVS Amino-acid change
XM_011537428.1:c.319-12313T= XP_011535730.1:n.319-12313T=
XR_943756.1:n.358+23750T=