Canonical Allele Identifier: CA495361476

Gene: PHKB

Linked Data

• MyVariant Identifiers: chr16:g.47732439C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.47698528C>G , CM000678.2:g.47698528C>G	GRCh38
NC_000016.9:g.47732439C>G , CM000678.1:g.47732439C>G	GRCh37
NC_000016.8:g.46289940C>G	NCBI36
NG_016598.1:g.242230C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696809.1:c.*1658C>G	ENSP00000512887.1:n.*1658C>G
ENST00000699276.1:c.*712C>G	ENSP00000514257.1:n.*712C>G
ENST00000323584.10:c.3084C>G MANE Select	ENSP00000313504.5:p.Val1028=
ENST00000299167.12:c.3084C>G	ENSP00000299167.8:p.Val1028=
ENST00000323584.9:c.3084C>G	ENSP00000313504.5:p.Val1028=
ENST00000564711.2:c.98C>G
ENST00000566044.5:c.3063C>G	ENSP00000456729.1:p.Val1021=
ENST00000566319.2:n.1900C>G
NM_000293.2:c.3084C>G	NP_000284.1:p.Val1028=
NM_001031835.2:c.3063C>G	NP_001027005.1:p.Val1021=
XM_005255983.3:c.3084C>G	XP_005256040.1:p.Val1028=
XM_005255984.3:c.3063C>G	XP_005256041.1:p.Val1021=
XM_011523107.1:c.1662C>G	XP_011521409.1:p.Val554=
NM_001363837.1:c.3084C>G	NP_001350766.1:p.Val1028=
XM_005255983.4:c.3084C>G	XP_005256040.1:p.Val1028=
XM_005255984.4:c.3063C>G	XP_005256041.1:p.Val1021=
XM_017023282.1:c.1971C>G	XP_016878771.1:p.Val657=
XM_017023283.1:c.1662C>G	XP_016878772.1:p.Val554=
XM_017023284.1:c.1662C>G	XP_016878773.1:p.Val554=
XR_001751913.1:n.3008C>G
NM_000293.3:c.3084C>G MANE Select	NP_000284.1:p.Val1028=
NM_001031835.3:c.3063C>G	NP_001027005.1:p.Val1021=