Canonical Allele Identifier: CA8013178
Gene: PHKG2 HGNC NCBI

Linked Data

dbSNP Id: rs775246080

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.30753405G>A , CM000678.2:g.30753405G>A GRCh38
NC_000016.9:g.30764726G>A , CM000678.1:g.30764726G>A GRCh37
NC_000016.8:g.30672227G>A NCBI36
NG_016616.1:g.10107G>A
NG_016616.2:g.10107G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000563588.6:c.404G>A MANE Select ENSP00000455607.1:p.Arg135Gln
ENST00000328273.11:c.404G>A ENSP00000329968.7:p.Arg135Gln
ENST00000424889.7:c.404G>A ENSP00000388571.3:p.Arg135Gln
ENST00000561712.1:c.78G>A
ENST00000563588.5:c.404G>A ENSP00000455607.1:p.Arg135Gln
ENST00000563607.1:c.*76G>A ENSP00000454641.1:n.*76G>A
ENST00000563913.5:n.737G>A
ENST00000564838.5:n.778G>A
ENST00000565897.5:c.404G>A ENSP00000457359.1:p.Arg135Gln
ENST00000565924.5:c.404G>A ENSP00000455091.1:p.Arg135Gln
ENST00000569684.1:n.816G>A
NM_000294.2:c.404G>A NP_000285.1:p.Arg135Gln
NM_001172432.1:c.404G>A NP_001165903.1:p.Arg135Gln
NM_000294.3:c.404G>A MANE Select NP_000285.1:p.Arg135Gln
NM_001172432.2:c.404G>A NP_001165903.1:p.Arg135Gln