Canonical Allele Identifier: CA2220492674
Gene: PHKB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.47696335C= , CM000678.2:g.47696335C= GRCh38
NC_000016.9:g.47730246C= , CM000678.1:g.47730246C= GRCh37
NC_000016.8:g.46287747C= NCBI36
NG_016598.1:g.240037C=

Transcript Alleles

HGVS Amino-acid change
ENST00000696809.1:c.*1470-46C= ENSP00000512887.1:n.*1470-46C=
ENST00000699276.1:c.*524-46C= ENSP00000514257.1:n.*524-46C=
ENST00000323584.10:c.2896-46C= MANE Select ENSP00000313504.5:n.2896-46C=
ENST00000299167.12:c.2896-46C= ENSP00000299167.8:n.2896-46C=
ENST00000323584.9:c.2896-46C= ENSP00000313504.5:n.2896-46C=
ENST00000566044.5:c.2875-46C= ENSP00000456729.1:n.2875-46C=
ENST00000566319.2:n.1712-46C=
NM_000293.2:c.2896-46C= NP_000284.1:n.2896-46C=
NM_001031835.2:c.2875-46C= NP_001027005.1:n.2875-46C=
XM_005255983.3:c.2896-46C= XP_005256040.1:n.2896-46C=
XM_005255984.3:c.2875-46C= XP_005256041.1:n.2875-46C=
XM_011523107.1:c.1474-46C= XP_011521409.1:n.1474-46C=
NM_001363837.1:c.2896-46C= NP_001350766.1:n.2896-46C=
XM_005255983.4:c.2896-46C= XP_005256040.1:n.2896-46C=
XM_005255984.4:c.2875-46C= XP_005256041.1:n.2875-46C=
XM_017023282.1:c.1783-46C= XP_016878771.1:n.1783-46C=
XM_017023283.1:c.1474-46C= XP_016878772.1:n.1474-46C=
XM_017023284.1:c.1474-46C= XP_016878773.1:n.1474-46C=
XR_001751913.1:n.2820-46C=
NM_000293.3:c.2896-46C= MANE Select NP_000284.1:n.2896-46C=
NM_001031835.3:c.2875-46C= NP_001027005.1:n.2875-46C=