Canonical Allele Identifier: CA2632771571

Gene: PHKG2

Linked Data

• gnomAD v4: 16-30756579-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.30756579G>T , CM000678.2:g.30756579G>T	GRCh38
NC_000016.9:g.30767900G>T , CM000678.1:g.30767900G>T	GRCh37
NC_000016.8:g.30675401G>T	NCBI36
NG_016616.1:g.13281G>T
NG_016616.2:g.13281G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000563588.6:c.802-11G>T MANE Select	ENSP00000455607.1:n.802-11G>T
ENST00000328273.11:c.814-11G>T	ENSP00000329968.7:n.814-11G>T
ENST00000424889.7:c.802-11G>T	ENSP00000388571.3:n.802-11G>T
ENST00000563588.5:c.802-11G>T	ENSP00000455607.1:n.802-11G>T
ENST00000563913.5:n.1135-11G>T
ENST00000564838.5:n.931-11G>T
NM_000294.2:c.802-11G>T	NP_000285.1:n.802-11G>T
NM_001172432.1:c.802-11G>T	NP_001165903.1:n.802-11G>T
NM_000294.3:c.802-11G>T MANE Select	NP_000285.1:n.802-11G>T
NM_001172432.2:c.802-11G>T	NP_001165903.1:n.802-11G>T