Canonical Allele Identifier: CA7263998

Gene: FAM161B COQ6

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.73950161A>G , CM000676.2:g.73950161A>G	GRCh38
NC_000014.8:g.74416864A>G , CM000676.1:g.74416864A>G	GRCh37
NC_000014.7:g.73486617A>G	NCBI36
NG_032805.1:g.5228A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000651776.1:c.55T>C (FAM161B)	ENSP00000499021.1:p.Trp19Arg
ENST00000286544.3:c.55T>C (FAM161B)	ENSP00000286544.3:p.Trp19Arg
ENST00000394026.8:c.69A>G (COQ6)	ENSP00000377594.4:p.Pro23=
ENST00000554341.6:c.69A>G (COQ6)	ENSP00000450736.2:p.Pro23=
NM_152445.2:c.55T>C (FAM161B)	NP_689658.2:p.Trp19Arg
NM_182480.2:c.69A>G (COQ6)	NP_872286.2:p.Pro23=
XM_011536475.1:c.55T>C (FAM161B)	XP_011534777.1:p.Trp19Arg
XM_011536809.1:c.-23A>G (COQ6)	XP_011535111.1:n.-23A>G
XM_011536475.2:c.55T>C (FAM161B)	XP_011534777.1:p.Trp19Arg
XM_011536809.3:c.-23A>G (COQ6)	XP_011535111.1:n.-23A>G
NM_182480.3:c.69A>G (COQ6)	NP_872286.2:p.Pro23=