Canonical Allele Identifier: CA396099579

Gene: PHKB

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.47511774T>A , CM000678.2:g.47511774T>A	GRCh38
NC_000016.9:g.47545685T>A , CM000678.1:g.47545685T>A	GRCh37
NC_000016.8:g.46103186T>A	NCBI36
NG_016598.1:g.55476T>A

Transcript Alleles

HGVS	Amino-acid Change
NM_000293.3:c.513+2T>A MANE Select	NP_000284.1:n.513+2T>A
ENST00000323584.10:c.513+2T>A MANE Select	ENSP00000313504.5:n.513+2T>A
NM_000293.2:c.513+2T>A	NP_000284.1:n.513+2T>A
NM_001031835.2:c.492+2T>A	NP_001027005.1:n.492+2T>A
NM_001031835.3:c.492+2T>A	NP_001027005.1:n.492+2T>A
NM_001363837.1:c.513+2T>A	NP_001350766.1:n.513+2T>A
ENST00000299167.12:c.513+2T>A	ENSP00000299167.8:n.513+2T>A
ENST00000323584.9:c.513+2T>A	ENSP00000313504.5:n.513+2T>A
ENST00000565424.2:n.97-35659T>A
ENST00000566037.6:c.492+2T>A	ENSP00000455664.2:n.492+2T>A
ENST00000566044.5:c.492+2T>A	ENSP00000456729.1:n.492+2T>A
ENST00000567402.5:n.528+2T>A
ENST00000570047.2:c.347+2T>A
ENST00000696809.1:c.492+2T>A	ENSP00000512887.1:n.492+2T>A
ENST00000699276.1:c.492+2T>A	ENSP00000514257.1:n.492+2T>A
XM_005255983.3:c.513+2T>A	XP_005256040.1:n.513+2T>A
XM_005255983.4:c.513+2T>A	XP_005256040.1:n.513+2T>A
XM_005255984.3:c.492+2T>A	XP_005256041.1:n.492+2T>A
XM_005255984.4:c.492+2T>A	XP_005256041.1:n.492+2T>A
XM_011523106.1:c.513+2T>A	XP_011521408.1:n.513+2T>A
XM_017023283.1:c.-993+2T>A	XP_016878772.1:n.-993+2T>A
XM_017023284.1:c.-993+2T>A	XP_016878773.1:n.-993+2T>A
XR_001751913.1:n.528+2T>A