Canonical Allele Identifier: CA2220394792
Gene: PHKB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.47596333G= , CM000678.2:g.47596333G= GRCh38
NC_000016.9:g.47630244G= , CM000678.1:g.47630244G= GRCh37
NC_000016.8:g.46187745G= NCBI36
NG_016598.1:g.140035G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000696809.1:c.1184-40G= ENSP00000512887.1:n.1184-40G=
ENST00000699276.1:c.1184-40G= ENSP00000514257.1:n.1184-40G=
ENST00000323584.10:c.1205-40G= MANE Select ENSP00000313504.5:n.1205-40G=
ENST00000299167.12:c.1205-40G= ENSP00000299167.8:n.1205-40G=
ENST00000323584.9:c.1205-40G= ENSP00000313504.5:n.1205-40G=
ENST00000566044.5:c.1184-40G= ENSP00000456729.1:n.1184-40G=
ENST00000566436.1:n.66-40G=
NM_000293.2:c.1205-40G= NP_000284.1:n.1205-40G=
NM_001031835.2:c.1184-40G= NP_001027005.1:n.1184-40G=
XM_005255983.3:c.1205-40G= XP_005256040.1:n.1205-40G=
XM_005255984.3:c.1184-40G= XP_005256041.1:n.1184-40G=
XM_011523106.1:c.1205-40G= XP_011521408.1:n.1205-40G=
NM_001363837.1:c.1205-40G= NP_001350766.1:n.1205-40G=
XM_005255983.4:c.1205-40G= XP_005256040.1:n.1205-40G=
XM_005255984.4:c.1184-40G= XP_005256041.1:n.1184-40G=
XM_017023282.1:c.92-40G= XP_016878771.1:n.92-40G=
XM_017023283.1:c.-301-40G= XP_016878772.1:n.-301-40G=
XM_017023284.1:c.-301-40G= XP_016878773.1:n.-301-40G=
XR_001751913.1:n.1220-40G=
NM_000293.3:c.1205-40G= MANE Select NP_000284.1:n.1205-40G=
NM_001031835.3:c.1184-40G= NP_001027005.1:n.1184-40G=