Canonical Allele Identifier: CA5617789

Gene: CYP2C8

Linked Data

• dbSNP Id: rs760313151
• ExAC: 10:96827005 C / G
• gnomAD v2: 10-96827005-C-G
• gnomAD v4: 10-95067248-C-G
• MyVariant Identifiers: chr10:g.96827005C>G (hg19) ; chr10:g.95067248C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.95067248C>G , CM000672.2:g.95067248C>G	GRCh38
NC_000010.10:g.96827005C>G , CM000672.1:g.96827005C>G	GRCh37
NC_000010.9:g.96816995C>G	NCBI36
NG_007972.1:g.7250G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371270.6:c.441G>C MANE Select	ENSP00000360317.3:p.Glu147Asp
ENST00000371270.5:c.441G>C	ENSP00000360317.3:p.Glu147Asp
ENST00000479946.2:n.745G>C
ENST00000490994.6:c.*227G>C	ENSP00000433314.1:n.*227G>C
ENST00000525991.5:c.*16G>C	ENSP00000433842.1:n.*16G>C
ENST00000526814.5:n.696G>C
ENST00000527420.5:c.441G>C	ENSP00000433191.1:p.Glu147Asp
ENST00000527953.5:n.696G>C
ENST00000533320.5:n.675G>C
ENST00000535898.5:c.135G>C	ENSP00000445062.1:p.Glu45Asp
ENST00000539050.5:c.231G>C	ENSP00000442343.2:p.Glu77Asp
ENST00000623108.3:c.231G>C	ENSP00000485110.1:p.Glu77Asp
ENST00000628935.1:c.183G>C	ENSP00000487145.1:p.Glu61Asp
NM_000770.3:c.441G>C MANE Select	NP_000761.3:p.Glu147Asp
NM_001198853.1:c.231G>C	NP_001185782.1:p.Glu77Asp
NM_001198854.1:c.135G>C	NP_001185783.1:p.Glu45Asp
NM_001198855.1:c.231G>C	NP_001185784.1:p.Glu77Asp
XR_945610.1:n.537G>C