Canonical Allele Identifier: CA2144473230
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.68807146A= , CM000676.2:g.68807146A= GRCh38
NC_000014.8:g.69273863A= , CM000676.1:g.69273863A= GRCh37
NC_000014.7:g.68343616A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XM_011537441.1:c.673-492T= XP_011535743.1:n.673-492T=
XM_011537442.1:c.673-492T= XP_011535744.1:n.673-492T=
XM_011537443.1:c.673-492T= XP_011535745.1:n.673-492T=