Canonical Allele Identifier: CA396101032

Gene: PHKB

Linked Data

• gnomAD v4: 16-47696401-G-T
• MyVariant Identifiers: chr16:g.47730312G>T (hg19) ; chr16:g.47696401G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.47696401G>T , CM000678.2:g.47696401G>T	GRCh38
NC_000016.9:g.47730312G>T , CM000678.1:g.47730312G>T	GRCh37
NC_000016.8:g.46287813G>T	NCBI36
NG_016598.1:g.240103G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696809.1:c.*1490G>T	ENSP00000512887.1:n.*1490G>T
ENST00000699276.1:c.*544G>T	ENSP00000514257.1:n.*544G>T
ENST00000323584.10:c.2916G>T MANE Select	ENSP00000313504.5:p.Met972Ile
ENST00000299167.12:c.2916G>T	ENSP00000299167.8:p.Met972Ile
ENST00000323584.9:c.2916G>T	ENSP00000313504.5:p.Met972Ile
ENST00000566044.5:c.2895G>T	ENSP00000456729.1:p.Met965Ile
ENST00000566319.2:n.1732G>T
NM_000293.2:c.2916G>T	NP_000284.1:p.Met972Ile
NM_001031835.2:c.2895G>T	NP_001027005.1:p.Met965Ile
XM_005255983.3:c.2916G>T	XP_005256040.1:p.Met972Ile
XM_005255984.3:c.2895G>T	XP_005256041.1:p.Met965Ile
XM_011523107.1:c.1494G>T	XP_011521409.1:p.Met498Ile
NM_001363837.1:c.2916G>T	NP_001350766.1:p.Met972Ile
XM_005255983.4:c.2916G>T	XP_005256040.1:p.Met972Ile
XM_005255984.4:c.2895G>T	XP_005256041.1:p.Met965Ile
XM_017023282.1:c.1803G>T	XP_016878771.1:p.Met601Ile
XM_017023283.1:c.1494G>T	XP_016878772.1:p.Met498Ile
XM_017023284.1:c.1494G>T	XP_016878773.1:p.Met498Ile
XR_001751913.1:n.2840G>T
NM_000293.3:c.2916G>T MANE Select	NP_000284.1:p.Met972Ile
NM_001031835.3:c.2895G>T	NP_001027005.1:p.Met965Ile