Canonical Allele Identifier: CA2220378112
Gene: PHKB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.47503037G= , CM000678.2:g.47503037G= GRCh38
NC_000016.9:g.47536948G= , CM000678.1:g.47536948G= GRCh37
NC_000016.8:g.46094449G= NCBI36
NG_016598.1:g.46739G=

Transcript Alleles

HGVS Amino-acid change
ENST00000696809.1:c.331G= ENSP00000512887.1:p.Ala111=
ENST00000699276.1:c.331G= ENSP00000514257.1:p.Ala111=
ENST00000323584.10:c.352G= MANE Select ENSP00000313504.5:p.Ala118=
ENST00000299167.12:c.352G= ENSP00000299167.8:p.Ala118=
ENST00000323584.9:c.352G= ENSP00000313504.5:p.Ala118=
ENST00000563376.5:c.331G= ENSP00000457905.1:p.Ala111=
ENST00000565424.2:n.96+41611G=
ENST00000566037.6:c.331G= ENSP00000455664.2:p.Ala111=
ENST00000566044.5:c.331G= ENSP00000456729.1:p.Ala111=
ENST00000567402.5:n.367G=
ENST00000570047.2:c.186G=
NM_000293.2:c.352G= NP_000284.1:p.Ala118=
NM_001031835.2:c.331G= NP_001027005.1:p.Ala111=
XM_005255983.3:c.352G= XP_005256040.1:p.Ala118=
XM_005255984.3:c.331G= XP_005256041.1:p.Ala111=
XM_011523106.1:c.352G= XP_011521408.1:p.Ala118=
NM_001363837.1:c.352G= NP_001350766.1:p.Ala118=
XM_005255983.4:c.352G= XP_005256040.1:p.Ala118=
XM_005255984.4:c.331G= XP_005256041.1:p.Ala111=
XM_017023283.1:c.-1154G= XP_016878772.1:n.-1154G=
XM_017023284.1:c.-1154G= XP_016878773.1:n.-1154G=
XR_001751913.1:n.367G=
NM_000293.3:c.352G= MANE Select NP_000284.1:p.Ala118=
NM_001031835.3:c.331G= NP_001027005.1:p.Ala111=