Canonical Allele Identifier: CA622170301

Gene: PHKG2

Linked Data

• dbSNP Id: rs1438113688
• gnomAD v2: 16-30764504-A-G
• gnomAD v4: 16-30753183-A-G
• MyVariant Identifiers: chr16:g.30764504A>G (hg19) ; chr16:g.30753183A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.30753183A>G , CM000678.2:g.30753183A>G	GRCh38
NC_000016.9:g.30764504A>G , CM000678.1:g.30764504A>G	GRCh37
NC_000016.8:g.30672005A>G	NCBI36
NG_016616.1:g.9885A>G
NG_016616.2:g.9885A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000563588.6:c.327-49A>G MANE Select	ENSP00000455607.1:n.327-49A>G
ENST00000328273.11:c.327-49A>G	ENSP00000329968.7:n.327-49A>G
ENST00000424889.7:c.327-49A>G	ENSP00000388571.3:n.327-49A>G
ENST00000563588.5:c.327-49A>G	ENSP00000455607.1:n.327-49A>G
ENST00000563607.1:c.263-49A>G	ENSP00000454641.1:n.263-49A>G
ENST00000563913.5:n.660-49A>G
ENST00000564838.5:n.701-49A>G
ENST00000565897.5:c.327-49A>G	ENSP00000457359.1:n.327-49A>G
ENST00000565924.5:c.327-49A>G	ENSP00000455091.1:n.327-49A>G
ENST00000569684.1:n.690A>G
NM_000294.2:c.327-49A>G	NP_000285.1:n.327-49A>G
NM_001172432.1:c.327-49A>G	NP_001165903.1:n.327-49A>G
NM_000294.3:c.327-49A>G MANE Select	NP_000285.1:n.327-49A>G
NM_001172432.2:c.327-49A>G	NP_001165903.1:n.327-49A>G