Canonical Allele Identifier: CA2523474954

Gene: PHKB

Linked Data

• gnomAD v4: 16-47696340-C-T

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.47696340C>T , CM000678.2:g.47696340C>T	GRCh38
NC_000016.9:g.47730251C>T , CM000678.1:g.47730251C>T	GRCh37
NC_000016.8:g.46287752C>T	NCBI36
NG_016598.1:g.240042C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000696809.1:c.*1470-41C>T	ENSP00000512887.1:n.*1470-41C>T
ENST00000699276.1:c.*524-41C>T	ENSP00000514257.1:n.*524-41C>T
ENST00000323584.10:c.2896-41C>T MANE Select	ENSP00000313504.5:n.2896-41C>T
ENST00000299167.12:c.2896-41C>T	ENSP00000299167.8:n.2896-41C>T
ENST00000323584.9:c.2896-41C>T	ENSP00000313504.5:n.2896-41C>T
ENST00000566044.5:c.2875-41C>T	ENSP00000456729.1:n.2875-41C>T
ENST00000566319.2:n.1712-41C>T
NM_000293.2:c.2896-41C>T	NP_000284.1:n.2896-41C>T
NM_001031835.2:c.2875-41C>T	NP_001027005.1:n.2875-41C>T
XM_005255983.3:c.2896-41C>T	XP_005256040.1:n.2896-41C>T
XM_005255984.3:c.2875-41C>T	XP_005256041.1:n.2875-41C>T
XM_011523107.1:c.1474-41C>T	XP_011521409.1:n.1474-41C>T
NM_001363837.1:c.2896-41C>T	NP_001350766.1:n.2896-41C>T
XM_005255983.4:c.2896-41C>T	XP_005256040.1:n.2896-41C>T
XM_005255984.4:c.2875-41C>T	XP_005256041.1:n.2875-41C>T
XM_017023282.1:c.1783-41C>T	XP_016878771.1:n.1783-41C>T
XM_017023283.1:c.1474-41C>T	XP_016878772.1:n.1474-41C>T
XM_017023284.1:c.1474-41C>T	XP_016878773.1:n.1474-41C>T
XR_001751913.1:n.2820-41C>T
NM_000293.3:c.2896-41C>T MANE Select	NP_000284.1:n.2896-41C>T
NM_001031835.3:c.2875-41C>T	NP_001027005.1:n.2875-41C>T