Canonical Allele Identifier: CA394427509

Gene: ZG16B

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.2830795A>C , CM000678.2:g.2830795A>C	GRCh38
NC_000016.9:g.2880796A>C , CM000678.1:g.2880796A>C	GRCh37
NC_000016.8:g.2820797A>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_145252.3:c.154A>C MANE Select	NP_660295.3:p.Ser52Arg
ENST00000382280.8:c.154A>C MANE Select	ENSP00000371715.4:p.Ser52Arg
NM_145252.2:c.262A>C	NP_660295.2:p.Ser88Arg
ENST00000382280.7:c.262A>C	ENSP00000371715.3:p.Ser88Arg
ENST00000570670.5:c.257A>C
ENST00000570670.6:c.154A>C	ENSP00000460793.2:p.Arg52=
ENST00000571723.1:c.204A>C
ENST00000571723.2:c.154A>C	ENSP00000458847.2:p.Arg52=
ENST00000572863.1:c.172A>C	ENSP00000461740.1:p.Ser58Arg
ENST00000572863.2:c.154A>C	ENSP00000461740.2:p.Ser52Arg
ENST00000573019.1:n.406A>C
ENST00000576423.1:n.415A>C