Canonical Allele Identifier: CA396101051
Gene: PHKB HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.47696410T>A , CM000678.2:g.47696410T>A GRCh38
NC_000016.9:g.47730321T>A , CM000678.1:g.47730321T>A GRCh37
NC_000016.8:g.46287822T>A NCBI36
NG_016598.1:g.240112T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000696809.1:c.*1499T>A ENSP00000512887.1:n.*1499T>A
ENST00000699276.1:c.*553T>A ENSP00000514257.1:n.*553T>A
ENST00000323584.10:c.2925T>A MANE Select ENSP00000313504.5:p.Tyr975Ter
ENST00000299167.12:c.2925T>A ENSP00000299167.8:p.Tyr975Ter
ENST00000323584.9:c.2925T>A ENSP00000313504.5:p.Tyr975Ter
ENST00000566044.5:c.2904T>A ENSP00000456729.1:p.Tyr968Ter
ENST00000566319.2:n.1741T>A
NM_000293.2:c.2925T>A NP_000284.1:p.Tyr975Ter
NM_001031835.2:c.2904T>A NP_001027005.1:p.Tyr968Ter
XM_005255983.3:c.2925T>A XP_005256040.1:p.Tyr975Ter
XM_005255984.3:c.2904T>A XP_005256041.1:p.Tyr968Ter
XM_011523107.1:c.1503T>A XP_011521409.1:p.Tyr501Ter
NM_001363837.1:c.2925T>A NP_001350766.1:p.Tyr975Ter
XM_005255983.4:c.2925T>A XP_005256040.1:p.Tyr975Ter
XM_005255984.4:c.2904T>A XP_005256041.1:p.Tyr968Ter
XM_017023282.1:c.1812T>A XP_016878771.1:p.Tyr604Ter
XM_017023283.1:c.1503T>A XP_016878772.1:p.Tyr501Ter
XM_017023284.1:c.1503T>A XP_016878773.1:p.Tyr501Ter
XR_001751913.1:n.2849T>A
NM_000293.3:c.2925T>A MANE Select NP_000284.1:p.Tyr975Ter
NM_001031835.3:c.2904T>A NP_001027005.1:p.Tyr968Ter