Canonical Allele Identifier: CA395658736

Gene: PHKG2

Linked Data

• dbSNP Id: rs1188632240
• gnomAD v2: 16-30767737-T-G
• gnomAD v4: 16-30756416-T-G
• MyVariant Identifiers: chr16:g.30767737T>G (hg19) ; chr16:g.30756416T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.30756416T>G , CM000678.2:g.30756416T>G	GRCh38
NC_000016.9:g.30767737T>G , CM000678.1:g.30767737T>G	GRCh37
NC_000016.8:g.30675238T>G	NCBI36
NG_016616.1:g.13118T>G
NG_016616.2:g.13118T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000563588.6:c.697T>G MANE Select	ENSP00000455607.1:p.Phe233Val
ENST00000328273.11:c.709T>G	ENSP00000329968.7:p.Phe237Val
ENST00000424889.7:c.697T>G	ENSP00000388571.3:p.Phe233Val
ENST00000563588.5:c.697T>G	ENSP00000455607.1:p.Phe233Val
ENST00000563913.5:n.1030T>G
ENST00000564838.5:n.931-174T>G
ENST00000565897.5:c.697T>G	ENSP00000457359.1:p.Phe233Val
ENST00000565924.5:c.697T>G	ENSP00000455091.1:p.Phe233Val
ENST00000569684.1:n.1121T>G
NM_000294.2:c.697T>G	NP_000285.1:p.Phe233Val
NM_001172432.1:c.697T>G	NP_001165903.1:p.Phe233Val
NM_000294.3:c.697T>G MANE Select	NP_000285.1:p.Phe233Val
NM_001172432.2:c.697T>G	NP_001165903.1:p.Phe233Val