Canonical Allele Identifier: CA3222227943

Gene: PHKG2

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.30751086C= , CM000678.2:g.30751086C=	GRCh38
NC_000016.9:g.30762407C= , CM000678.1:g.30762407C=	GRCh37
NC_000016.8:g.30669908C=	NCBI36
NG_016616.1:g.7788C=
NG_016616.2:g.7788C=

Transcript Alleles

HGVS	Amino-acid Change
NM_000294.3:c.96-20C= MANE Select	NP_000285.1:n.96-20C=
ENST00000563588.6:c.96-20C= MANE Select	ENSP00000455607.1:n.96-20C=
NM_000294.2:c.96-20C=	NP_000285.1:n.96-20C=
NM_001172432.1:c.96-20C=	NP_001165903.1:n.96-20C=
NM_001172432.2:c.96-20C=	NP_001165903.1:n.96-20C=
ENST00000328273.11:c.96-20C=	ENSP00000329968.7:n.96-20C=
ENST00000424889.7:c.96-20C=	ENSP00000388571.3:n.96-20C=
ENST00000563588.5:c.96-20C=	ENSP00000455607.1:n.96-20C=
ENST00000563607.1:c.96-20C=	ENSP00000454641.1:n.96-20C=
ENST00000563913.5:n.162-20C=
ENST00000564838.5:n.203-20C=
ENST00000565897.5:c.96-20C=	ENSP00000457359.1:n.96-20C=
ENST00000565924.5:c.96-20C=	ENSP00000455091.1:n.96-20C=
ENST00000569762.1:n.73-20C=