Canonical Allele Identifier: CA495073115

Gene: PHKB

Linked Data

• MyVariant Identifiers: chr16:g.47630345T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.47596434T>C , CM000678.2:g.47596434T>C	GRCh38
NC_000016.9:g.47630345T>C , CM000678.1:g.47630345T>C	GRCh37
NC_000016.8:g.46187846T>C	NCBI36
NG_016598.1:g.140136T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696809.1:c.1245T>C	ENSP00000512887.1:p.Asn415=
ENST00000699276.1:c.1245T>C	ENSP00000514257.1:p.Asn415=
ENST00000323584.10:c.1266T>C MANE Select	ENSP00000313504.5:p.Asn422=
ENST00000299167.12:c.1266T>C	ENSP00000299167.8:p.Asn422=
ENST00000323584.9:c.1266T>C	ENSP00000313504.5:p.Asn422=
ENST00000566044.5:c.1245T>C	ENSP00000456729.1:p.Asn415=
ENST00000566436.1:n.127T>C
ENST00000568439.1:c.7T>C
NM_000293.2:c.1266T>C	NP_000284.1:p.Asn422=
NM_001031835.2:c.1245T>C	NP_001027005.1:p.Asn415=
XM_005255983.3:c.1266T>C	XP_005256040.1:p.Asn422=
XM_005255984.3:c.1245T>C	XP_005256041.1:p.Asn415=
XM_011523106.1:c.1266T>C	XP_011521408.1:p.Asn422=
NM_001363837.1:c.1266T>C	NP_001350766.1:p.Asn422=
XM_005255983.4:c.1266T>C	XP_005256040.1:p.Asn422=
XM_005255984.4:c.1245T>C	XP_005256041.1:p.Asn415=
XM_017023282.1:c.153T>C	XP_016878771.1:p.Asn51=
XM_017023283.1:c.-240T>C	XP_016878772.1:n.-240T>C
XM_017023284.1:c.-240T>C	XP_016878773.1:n.-240T>C
XR_001751913.1:n.1281T>C
NM_000293.3:c.1266T>C MANE Select	NP_000284.1:p.Asn422=
NM_001031835.3:c.1245T>C	NP_001027005.1:p.Asn415=