Canonical Allele Identifier: CA2220483869

Gene: PHKB

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.47650940G= , CM000678.2:g.47650940G=	GRCh38
NC_000016.9:g.47684851G= , CM000678.1:g.47684851G=	GRCh37
NC_000016.8:g.46242352G=	NCBI36
NG_016598.1:g.194642G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000696809.1:c.*545+19G=	ENSP00000512887.1:n.*545+19G=
ENST00000699276.1:c.1950+19G=	ENSP00000514257.1:n.1950+19G=
ENST00000323584.10:c.1971+19G= MANE Select	ENSP00000313504.5:n.1971+19G=
ENST00000299167.12:c.1971+19G=	ENSP00000299167.8:n.1971+19G=
ENST00000323584.9:c.1971+19G=	ENSP00000313504.5:n.1971+19G=
ENST00000566044.5:c.1950+19G=	ENSP00000456729.1:n.1950+19G=
ENST00000568171.1:n.92+19G=
NM_000293.2:c.1971+19G=	NP_000284.1:n.1971+19G=
NM_001031835.2:c.1950+19G=	NP_001027005.1:n.1950+19G=
XM_005255983.3:c.1971+19G=	XP_005256040.1:n.1971+19G=
XM_005255984.3:c.1950+19G=	XP_005256041.1:n.1950+19G=
XM_011523106.1:c.1971+19G=	XP_011521408.1:n.1971+19G=
XM_011523107.1:c.549+19G=	XP_011521409.1:n.549+19G=
NM_001363837.1:c.1971+19G=	NP_001350766.1:n.1971+19G=
XM_005255983.4:c.1971+19G=	XP_005256040.1:n.1971+19G=
XM_005255984.4:c.1950+19G=	XP_005256041.1:n.1950+19G=
XM_017023282.1:c.858+19G=	XP_016878771.1:n.858+19G=
XM_017023283.1:c.549+19G=	XP_016878772.1:n.549+19G=
XM_017023284.1:c.549+19G=	XP_016878773.1:n.549+19G=
XR_001751913.1:n.1986+19G=
NM_000293.3:c.1971+19G= MANE Select	NP_000284.1:n.1971+19G=
NM_001031835.3:c.1950+19G=	NP_001027005.1:n.1950+19G=