Canonical Allele Identifier: CA2575971669

Gene: PHKG2

Linked Data

• gnomAD v4: 16-30753580-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.30753580T>C , CM000678.2:g.30753580T>C	GRCh38
NC_000016.9:g.30764901T>C , CM000678.1:g.30764901T>C	GRCh37
NC_000016.8:g.30672402T>C	NCBI36
NG_016616.1:g.10282T>C
NG_016616.2:g.10282T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000563588.6:c.556+23T>C MANE Select	ENSP00000455607.1:n.556+23T>C
ENST00000328273.11:c.556+23T>C	ENSP00000329968.7:n.556+23T>C
ENST00000424889.7:c.556+23T>C	ENSP00000388571.3:n.556+23T>C
ENST00000561712.1:c.230+23T>C
ENST00000563588.5:c.556+23T>C	ENSP00000455607.1:n.556+23T>C
ENST00000563913.5:n.889+23T>C
ENST00000564838.5:n.930+23T>C
ENST00000565897.5:c.556+23T>C	ENSP00000457359.1:n.556+23T>C
ENST00000565924.5:c.556+23T>C	ENSP00000455091.1:n.556+23T>C
ENST00000569684.1:n.968+23T>C
NM_000294.2:c.556+23T>C	NP_000285.1:n.556+23T>C
NM_001172432.1:c.556+23T>C	NP_001165903.1:n.556+23T>C
NM_000294.3:c.556+23T>C MANE Select	NP_000285.1:n.556+23T>C
NM_001172432.2:c.556+23T>C	NP_001165903.1:n.556+23T>C