Canonical Allele Identifier: CA2144473234
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.68807148C= , CM000676.2:g.68807148C= GRCh38
NC_000014.8:g.69273865C= , CM000676.1:g.69273865C= GRCh37
NC_000014.7:g.68343618C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XM_011537441.1:c.673-494G= XP_011535743.1:n.673-494G=
XM_011537442.1:c.673-494G= XP_011535744.1:n.673-494G=
XM_011537443.1:c.673-494G= XP_011535745.1:n.673-494G=