Canonical Allele Identifier: CA2633049967

Gene: PHKB

Linked Data

• gnomAD v4: 16-47696503-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.47696503A>G , CM000678.2:g.47696503A>G	GRCh38
NC_000016.9:g.47730414A>G , CM000678.1:g.47730414A>G	GRCh37
NC_000016.8:g.46287915A>G	NCBI36
NG_016598.1:g.240205A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696809.1:c.*1577+15A>G	ENSP00000512887.1:n.*1577+15A>G
ENST00000699276.1:c.*631+15A>G	ENSP00000514257.1:n.*631+15A>G
ENST00000323584.10:c.3003+15A>G MANE Select	ENSP00000313504.5:n.3003+15A>G
ENST00000299167.12:c.3003+15A>G	ENSP00000299167.8:n.3003+15A>G
ENST00000323584.9:c.3003+15A>G	ENSP00000313504.5:n.3003+15A>G
ENST00000564711.2:c.17+15A>G
ENST00000566044.5:c.2982+15A>G	ENSP00000456729.1:n.2982+15A>G
ENST00000566319.2:n.1819+15A>G
NM_000293.2:c.3003+15A>G	NP_000284.1:n.3003+15A>G
NM_001031835.2:c.2982+15A>G	NP_001027005.1:n.2982+15A>G
XM_005255983.3:c.3003+15A>G	XP_005256040.1:n.3003+15A>G
XM_005255984.3:c.2982+15A>G	XP_005256041.1:n.2982+15A>G
XM_011523107.1:c.1581+15A>G	XP_011521409.1:n.1581+15A>G
NM_001363837.1:c.3003+15A>G	NP_001350766.1:n.3003+15A>G
XM_005255983.4:c.3003+15A>G	XP_005256040.1:n.3003+15A>G
XM_005255984.4:c.2982+15A>G	XP_005256041.1:n.2982+15A>G
XM_017023282.1:c.1890+15A>G	XP_016878771.1:n.1890+15A>G
XM_017023283.1:c.1581+15A>G	XP_016878772.1:n.1581+15A>G
XM_017023284.1:c.1581+15A>G	XP_016878773.1:n.1581+15A>G
XR_001751913.1:n.2927+15A>G
NM_000293.3:c.3003+15A>G MANE Select	NP_000284.1:n.3003+15A>G
NM_001031835.3:c.2982+15A>G	NP_001027005.1:n.2982+15A>G