Canonical Allele Identifier: CA2216726234

Gene: PHKG2

Linked Data

• dbSNP Id: rs2053380915

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.30753626G>C , CM000678.2:g.30753626G>C	GRCh38
NC_000016.9:g.30764947G>C , CM000678.1:g.30764947G>C	GRCh37
NC_000016.8:g.30672448G>C	NCBI36
NG_016616.1:g.10328G>C
NG_016616.2:g.10328G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000563588.6:c.556+69G>C MANE Select	ENSP00000455607.1:n.556+69G>C
ENST00000328273.11:c.556+69G>C	ENSP00000329968.7:n.556+69G>C
ENST00000424889.7:c.556+69G>C	ENSP00000388571.3:n.556+69G>C
ENST00000561712.1:c.230+69G>C
ENST00000563588.5:c.556+69G>C	ENSP00000455607.1:n.556+69G>C
ENST00000563913.5:n.889+69G>C
ENST00000564838.5:n.930+69G>C
ENST00000565897.5:c.556+69G>C	ENSP00000457359.1:n.556+69G>C
ENST00000565924.5:c.556+69G>C	ENSP00000455091.1:n.556+69G>C
ENST00000569684.1:n.968+69G>C
NM_000294.2:c.556+69G>C	NP_000285.1:n.556+69G>C
NM_001172432.1:c.556+69G>C	NP_001165903.1:n.556+69G>C
NM_000294.3:c.556+69G>C MANE Select	NP_000285.1:n.556+69G>C
NM_001172432.2:c.556+69G>C	NP_001165903.1:n.556+69G>C