Canonical Allele Identifier: CA494912376

Gene: PHKG2

Linked Data

• dbSNP Id: rs2151310303
• COSMIC: COSM3113086
• MyVariant Identifiers: chr16:g.30767712C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.30756391C>T , CM000678.2:g.30756391C>T	GRCh38
NC_000016.9:g.30767712C>T , CM000678.1:g.30767712C>T	GRCh37
NC_000016.8:g.30675213C>T	NCBI36
NG_016616.1:g.13093C>T
NG_016616.2:g.13093C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000563588.6:c.672C>T MANE Select	ENSP00000455607.1:p.Phe224=
ENST00000328273.11:c.684C>T	ENSP00000329968.7:p.Phe228=
ENST00000424889.7:c.672C>T	ENSP00000388571.3:p.Phe224=
ENST00000563588.5:c.672C>T	ENSP00000455607.1:p.Phe224=
ENST00000563913.5:n.1005C>T
ENST00000564838.5:n.931-199C>T
ENST00000565897.5:c.672C>T	ENSP00000457359.1:p.Phe224=
ENST00000565924.5:c.672C>T	ENSP00000455091.1:p.Phe224=
ENST00000569684.1:n.1096C>T
NM_000294.2:c.672C>T	NP_000285.1:p.Phe224=
NM_001172432.1:c.672C>T	NP_001165903.1:p.Phe224=
NM_000294.3:c.672C>T MANE Select	NP_000285.1:p.Phe224=
NM_001172432.2:c.672C>T	NP_001165903.1:p.Phe224=