Canonical Allele Identifier: CA1997283773
Community Standard Title: NC_000011.10:g.105052348A=
Gene: CARD16 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.105052348A= , CM000673.2:g.105052348A= GRCh38
NC_000011.9:g.104923075A= , CM000673.1:g.104923075A= GRCh37
NC_000011.8:g.104428285A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000525374.1:c.8-7690T= ENSP00000433700.1:n.8-7690T=
XR_001748352.1:n.164+4185A=