Canonical Allele Identifier: CA395658662

Gene: PHKG2

Linked Data

• dbSNP Id: rs1292727809
• gnomAD v2: 16-30767711-T-C
• gnomAD v4: 16-30756390-T-C
• MyVariant Identifiers: chr16:g.30767711T>C (hg19) ; chr16:g.30756390T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.30756390T>C , CM000678.2:g.30756390T>C	GRCh38
NC_000016.9:g.30767711T>C , CM000678.1:g.30767711T>C	GRCh37
NC_000016.8:g.30675212T>C	NCBI36
NG_016616.1:g.13092T>C
NG_016616.2:g.13092T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000563588.6:c.671T>C MANE Select	ENSP00000455607.1:p.Phe224Ser
ENST00000328273.11:c.683T>C	ENSP00000329968.7:p.Phe228Ser
ENST00000424889.7:c.671T>C	ENSP00000388571.3:p.Phe224Ser
ENST00000563588.5:c.671T>C	ENSP00000455607.1:p.Phe224Ser
ENST00000563913.5:n.1004T>C
ENST00000564838.5:n.931-200T>C
ENST00000565897.5:c.671T>C	ENSP00000457359.1:p.Phe224Ser
ENST00000565924.5:c.671T>C	ENSP00000455091.1:p.Phe224Ser
ENST00000569684.1:n.1095T>C
NM_000294.2:c.671T>C	NP_000285.1:p.Phe224Ser
NM_001172432.1:c.671T>C	NP_001165903.1:p.Phe224Ser
NM_000294.3:c.671T>C MANE Select	NP_000285.1:p.Phe224Ser
NM_001172432.2:c.671T>C	NP_001165903.1:p.Phe224Ser