Canonical Allele Identifier: CA494684084

Gene: PHKG2

Linked Data

• dbSNP Id: rs773982918
• gnomAD v4: 16-30753236-C-A
• MyVariant Identifiers: chr16:g.30764557C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.30753236C>A , CM000678.2:g.30753236C>A	GRCh38
NC_000016.9:g.30764557C>A , CM000678.1:g.30764557C>A	GRCh37
NC_000016.8:g.30672058C>A	NCBI36
NG_016616.1:g.9938C>A
NG_016616.2:g.9938C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000563588.6:c.331C>A MANE Select	ENSP00000455607.1:p.Arg111=
ENST00000328273.11:c.331C>A	ENSP00000329968.7:p.Arg111=
ENST00000424889.7:c.331C>A	ENSP00000388571.3:p.Arg111=
ENST00000561712.1:c.5C>A
ENST00000563588.5:c.331C>A	ENSP00000455607.1:p.Arg111=
ENST00000563607.1:c.*3C>A	ENSP00000454641.1:n.*3C>A
ENST00000563913.5:n.664C>A
ENST00000564838.5:n.705C>A
ENST00000565897.5:c.331C>A	ENSP00000457359.1:p.Arg111=
ENST00000565924.5:c.331C>A	ENSP00000455091.1:p.Arg111=
ENST00000569684.1:n.743C>A
NM_000294.2:c.331C>A	NP_000285.1:p.Arg111=
NM_001172432.1:c.331C>A	NP_001165903.1:p.Arg111=
NM_000294.3:c.331C>A MANE Select	NP_000285.1:p.Arg111=
NM_001172432.2:c.331C>A	NP_001165903.1:p.Arg111=