Canonical Allele Identifier: CA8040566

Gene: PHKB

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.47547534A>G , CM000678.2:g.47547534A>G	GRCh38
NC_000016.9:g.47581445A>G , CM000678.1:g.47581445A>G	GRCh37
NC_000016.8:g.46138946A>G	NCBI36
NG_016598.1:g.91236A>G

Transcript Alleles

HGVS	Amino-acid Change
NM_000293.3:c.696A>G MANE Select	NP_000284.1:p.Thr232=
ENST00000323584.10:c.696A>G MANE Select	ENSP00000313504.5:p.Thr232=
NM_000293.2:c.696A>G	NP_000284.1:p.Thr232=
NM_001031835.2:c.675A>G	NP_001027005.1:p.Thr225=
NM_001031835.3:c.675A>G	NP_001027005.1:p.Thr225=
NM_001363837.1:c.696A>G	NP_001350766.1:p.Thr232=
ENST00000299167.12:c.696A>G	ENSP00000299167.8:p.Thr232=
ENST00000323584.9:c.696A>G	ENSP00000313504.5:p.Thr232=
ENST00000565424.2:n.198A>G
ENST00000566037.6:c.675A>G	ENSP00000455664.2:p.Thr225=
ENST00000566044.5:c.675A>G	ENSP00000456729.1:p.Thr225=
ENST00000567402.5:n.711A>G
ENST00000570047.2:c.530A>G
ENST00000696809.1:c.675A>G	ENSP00000512887.1:p.Thr225=
ENST00000699276.1:c.675A>G	ENSP00000514257.1:p.Thr225=
XM_005255983.3:c.696A>G	XP_005256040.1:p.Thr232=
XM_005255983.4:c.696A>G	XP_005256040.1:p.Thr232=
XM_005255984.3:c.675A>G	XP_005256041.1:p.Thr225=
XM_005255984.4:c.675A>G	XP_005256041.1:p.Thr225=
XM_011523106.1:c.696A>G	XP_011521408.1:p.Thr232=
XM_017023283.1:c.-810A>G	XP_016878772.1:n.-810A>G
XM_017023284.1:c.-810A>G	XP_016878773.1:n.-810A>G
XR_001751913.1:n.711A>G