Canonical Allele Identifier: CA495361419

Gene: PHKB

Linked Data

• gnomAD v4: 16-47696485-A-G
• MyVariant Identifiers: chr16:g.47730396A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.47696485A>G , CM000678.2:g.47696485A>G	GRCh38
NC_000016.9:g.47730396A>G , CM000678.1:g.47730396A>G	GRCh37
NC_000016.8:g.46287897A>G	NCBI36
NG_016598.1:g.240187A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696809.1:c.*1574A>G	ENSP00000512887.1:n.*1574A>G
ENST00000699276.1:c.*628A>G	ENSP00000514257.1:n.*628A>G
ENST00000323584.10:c.3000A>G MANE Select	ENSP00000313504.5:p.Val1000=
ENST00000299167.12:c.3000A>G	ENSP00000299167.8:p.Val1000=
ENST00000323584.9:c.3000A>G	ENSP00000313504.5:p.Val1000=
ENST00000564711.2:c.14A>G
ENST00000566044.5:c.2979A>G	ENSP00000456729.1:p.Val993=
ENST00000566319.2:n.1816A>G
NM_000293.2:c.3000A>G	NP_000284.1:p.Val1000=
NM_001031835.2:c.2979A>G	NP_001027005.1:p.Val993=
XM_005255983.3:c.3000A>G	XP_005256040.1:p.Val1000=
XM_005255984.3:c.2979A>G	XP_005256041.1:p.Val993=
XM_011523107.1:c.1578A>G	XP_011521409.1:p.Val526=
NM_001363837.1:c.3000A>G	NP_001350766.1:p.Val1000=
XM_005255983.4:c.3000A>G	XP_005256040.1:p.Val1000=
XM_005255984.4:c.2979A>G	XP_005256041.1:p.Val993=
XM_017023282.1:c.1887A>G	XP_016878771.1:p.Val629=
XM_017023283.1:c.1578A>G	XP_016878772.1:p.Val526=
XM_017023284.1:c.1578A>G	XP_016878773.1:p.Val526=
XR_001751913.1:n.2924A>G
NM_000293.3:c.3000A>G MANE Select	NP_000284.1:p.Val1000=
NM_001031835.3:c.2979A>G	NP_001027005.1:p.Val993=