Canonical Allele Identifier: CA2220483774
Gene: PHKB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.47650839G= , CM000678.2:g.47650839G= GRCh38
NC_000016.9:g.47684750G= , CM000678.1:g.47684750G= GRCh37
NC_000016.8:g.46242251G= NCBI36
NG_016598.1:g.194541G=

Transcript Alleles

HGVS Amino-acid change
ENST00000696809.1:c.*463G= ENSP00000512887.1:n.*463G=
ENST00000699276.1:c.1868G= ENSP00000514257.1:p.Arg623=
ENST00000323584.10:c.1889G= MANE Select ENSP00000313504.5:p.Arg630=
ENST00000299167.12:c.1889G= ENSP00000299167.8:p.Arg630=
ENST00000323584.9:c.1889G= ENSP00000313504.5:p.Arg630=
ENST00000566044.5:c.1868G= ENSP00000456729.1:p.Arg623=
ENST00000568171.1:n.10G=
NM_000293.2:c.1889G= NP_000284.1:p.Arg630=
NM_001031835.2:c.1868G= NP_001027005.1:p.Arg623=
XM_005255983.3:c.1889G= XP_005256040.1:p.Arg630=
XM_005255984.3:c.1868G= XP_005256041.1:p.Arg623=
XM_011523106.1:c.1889G= XP_011521408.1:p.Arg630=
XM_011523107.1:c.467G= XP_011521409.1:p.Arg156=
NM_001363837.1:c.1889G= NP_001350766.1:p.Arg630=
XM_005255983.4:c.1889G= XP_005256040.1:p.Arg630=
XM_005255984.4:c.1868G= XP_005256041.1:p.Arg623=
XM_017023282.1:c.776G= XP_016878771.1:p.Arg259=
XM_017023283.1:c.467G= XP_016878772.1:p.Arg156=
XM_017023284.1:c.467G= XP_016878773.1:p.Arg156=
XR_001751913.1:n.1904G=
NM_000293.3:c.1889G= MANE Select NP_000284.1:p.Arg630=
NM_001031835.3:c.1868G= NP_001027005.1:p.Arg623=