Canonical Allele Identifier: CA2740093306

Gene: PHKG2

Linked Data

• ClinVar Variation Id: 3005863
• ClinVar RCV Id: RCV003863950

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.30753316G>T , CM000678.2:g.30753316G>T	GRCh38
NC_000016.9:g.30764637G>T , CM000678.1:g.30764637G>T	GRCh37
NC_000016.8:g.30672138G>T	NCBI36
NG_016616.1:g.10018G>T
NG_016616.2:g.10018G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000563588.6:c.392+19G>T MANE Select	ENSP00000455607.1:n.392+19G>T
ENST00000328273.11:c.392+19G>T	ENSP00000329968.7:n.392+19G>T
ENST00000424889.7:c.392+19G>T	ENSP00000388571.3:n.392+19G>T
ENST00000561712.1:c.66+19G>T
ENST00000563588.5:c.392+19G>T	ENSP00000455607.1:n.392+19G>T
ENST00000563607.1:c.*64+19G>T	ENSP00000454641.1:n.*64+19G>T
ENST00000563913.5:n.725+19G>T
ENST00000564838.5:n.766+19G>T
ENST00000565897.5:c.392+19G>T	ENSP00000457359.1:n.392+19G>T
ENST00000565924.5:c.392+19G>T	ENSP00000455091.1:n.392+19G>T
ENST00000569684.1:n.804+19G>T
NM_000294.2:c.392+19G>T	NP_000285.1:n.392+19G>T
NM_001172432.1:c.392+19G>T	NP_001165903.1:n.392+19G>T
NM_000294.3:c.392+19G>T MANE Select	NP_000285.1:n.392+19G>T
NM_001172432.2:c.392+19G>T	NP_001165903.1:n.392+19G>T