Canonical Allele Identifier: CA396101022

Gene: PHKB

Linked Data

• MyVariant Identifiers: chr16:g.47730309T>G (hg19) ; chr16:g.47696398T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.47696398T>G , CM000678.2:g.47696398T>G	GRCh38
NC_000016.9:g.47730309T>G , CM000678.1:g.47730309T>G	GRCh37
NC_000016.8:g.46287810T>G	NCBI36
NG_016598.1:g.240100T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696809.1:c.*1487T>G	ENSP00000512887.1:n.*1487T>G
ENST00000699276.1:c.*541T>G	ENSP00000514257.1:n.*541T>G
ENST00000323584.10:c.2913T>G MANE Select	ENSP00000313504.5:p.Asp971Glu
ENST00000299167.12:c.2913T>G	ENSP00000299167.8:p.Asp971Glu
ENST00000323584.9:c.2913T>G	ENSP00000313504.5:p.Asp971Glu
ENST00000566044.5:c.2892T>G	ENSP00000456729.1:p.Asp964Glu
ENST00000566319.2:n.1729T>G
NM_000293.2:c.2913T>G	NP_000284.1:p.Asp971Glu
NM_001031835.2:c.2892T>G	NP_001027005.1:p.Asp964Glu
XM_005255983.3:c.2913T>G	XP_005256040.1:p.Asp971Glu
XM_005255984.3:c.2892T>G	XP_005256041.1:p.Asp964Glu
XM_011523107.1:c.1491T>G	XP_011521409.1:p.Asp497Glu
NM_001363837.1:c.2913T>G	NP_001350766.1:p.Asp971Glu
XM_005255983.4:c.2913T>G	XP_005256040.1:p.Asp971Glu
XM_005255984.4:c.2892T>G	XP_005256041.1:p.Asp964Glu
XM_017023282.1:c.1800T>G	XP_016878771.1:p.Asp600Glu
XM_017023283.1:c.1491T>G	XP_016878772.1:p.Asp497Glu
XM_017023284.1:c.1491T>G	XP_016878773.1:p.Asp497Glu
XR_001751913.1:n.2837T>G
NM_000293.3:c.2913T>G MANE Select	NP_000284.1:p.Asp971Glu
NM_001031835.3:c.2892T>G	NP_001027005.1:p.Asp964Glu