Canonical Allele Identifier: CA2632771571
Gene: PHKG2 HGNC NCBI

Linked Data

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