Canonical Allele Identifier: CA2220492637

Gene: PHKB

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.47696208G= , CM000678.2:g.47696208G=	GRCh38
NC_000016.9:g.47730119G= , CM000678.1:g.47730119G=	GRCh37
NC_000016.8:g.46287620G=	NCBI36
NG_016598.1:g.239910G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696809.1:c.*1470-173G=	ENSP00000512887.1:n.*1470-173G=
ENST00000699276.1:c.*524-173G=	ENSP00000514257.1:n.*524-173G=
ENST00000323584.10:c.2896-173G= MANE Select	ENSP00000313504.5:n.2896-173G=
ENST00000299167.12:c.2896-173G=	ENSP00000299167.8:n.2896-173G=
ENST00000323584.9:c.2896-173G=	ENSP00000313504.5:n.2896-173G=
ENST00000566044.5:c.2875-173G=	ENSP00000456729.1:n.2875-173G=
ENST00000566319.2:n.1712-173G=
NM_000293.2:c.2896-173G=	NP_000284.1:n.2896-173G=
NM_001031835.2:c.2875-173G=	NP_001027005.1:n.2875-173G=
XM_005255983.3:c.2896-173G=	XP_005256040.1:n.2896-173G=
XM_005255984.3:c.2875-173G=	XP_005256041.1:n.2875-173G=
XM_011523107.1:c.1474-173G=	XP_011521409.1:n.1474-173G=
NM_001363837.1:c.2896-173G=	NP_001350766.1:n.2896-173G=
XM_005255983.4:c.2896-173G=	XP_005256040.1:n.2896-173G=
XM_005255984.4:c.2875-173G=	XP_005256041.1:n.2875-173G=
XM_017023282.1:c.1783-173G=	XP_016878771.1:n.1783-173G=
XM_017023283.1:c.1474-173G=	XP_016878772.1:n.1474-173G=
XM_017023284.1:c.1474-173G=	XP_016878773.1:n.1474-173G=
XR_001751913.1:n.2820-173G=
NM_000293.3:c.2896-173G= MANE Select	NP_000284.1:n.2896-173G=
NM_001031835.3:c.2875-173G=	NP_001027005.1:n.2875-173G=