Canonical Allele Identifier: CA396099022
Gene: PHKB HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.47503044A>C , CM000678.2:g.47503044A>C GRCh38
NC_000016.9:g.47536955A>C , CM000678.1:g.47536955A>C GRCh37
NC_000016.8:g.46094456A>C NCBI36
NG_016598.1:g.46746A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000696809.1:c.338A>C ENSP00000512887.1:p.Lys113Thr
ENST00000699276.1:c.338A>C ENSP00000514257.1:p.Lys113Thr
ENST00000323584.10:c.359A>C MANE Select ENSP00000313504.5:p.Lys120Thr
ENST00000299167.12:c.359A>C ENSP00000299167.8:p.Lys120Thr
ENST00000323584.9:c.359A>C ENSP00000313504.5:p.Lys120Thr
ENST00000563376.5:c.338A>C ENSP00000457905.1:p.Lys113Thr
ENST00000565424.2:n.96+41618A>C
ENST00000566037.6:c.338A>C ENSP00000455664.2:p.Lys113Thr
ENST00000566044.5:c.338A>C ENSP00000456729.1:p.Lys113Thr
ENST00000567402.5:n.374A>C
ENST00000570047.2:c.193A>C
NM_000293.2:c.359A>C NP_000284.1:p.Lys120Thr
NM_001031835.2:c.338A>C NP_001027005.1:p.Lys113Thr
XM_005255983.3:c.359A>C XP_005256040.1:p.Lys120Thr
XM_005255984.3:c.338A>C XP_005256041.1:p.Lys113Thr
XM_011523106.1:c.359A>C XP_011521408.1:p.Lys120Thr
NM_001363837.1:c.359A>C NP_001350766.1:p.Lys120Thr
XM_005255983.4:c.359A>C XP_005256040.1:p.Lys120Thr
XM_005255984.4:c.338A>C XP_005256041.1:p.Lys113Thr
XM_017023283.1:c.-1147A>C XP_016878772.1:n.-1147A>C
XM_017023284.1:c.-1147A>C XP_016878773.1:n.-1147A>C
XR_001751913.1:n.374A>C
NM_000293.3:c.359A>C MANE Select NP_000284.1:p.Lys120Thr
NM_001031835.3:c.338A>C NP_001027005.1:p.Lys113Thr