Canonical Allele Identifier: CA5617791

Gene: CYP2C8

Linked Data

• dbSNP Id: rs540288649
• ExAC: 10:96827016 G / C
• gnomAD v2: 10-96827016-G-C
• gnomAD v3: 10-95067259-G-C
• gnomAD v4: 10-95067259-G-C
• MyVariant Identifiers: chr10:g.96827016G>C (hg19) ; chr10:g.95067259G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.95067259G>C , CM000672.2:g.95067259G>C	GRCh38
NC_000010.10:g.96827016G>C , CM000672.1:g.96827016G>C	GRCh37
NC_000010.9:g.96817006G>C	NCBI36
NG_007972.1:g.7239C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371270.6:c.430C>G MANE Select	ENSP00000360317.3:p.Arg144Gly
ENST00000371270.5:c.430C>G	ENSP00000360317.3:p.Arg144Gly
ENST00000479946.2:n.734C>G
ENST00000490994.6:c.*216C>G	ENSP00000433314.1:n.*216C>G
ENST00000525991.5:c.*5C>G	ENSP00000433842.1:n.*5C>G
ENST00000526814.5:n.685C>G
ENST00000527420.5:c.430C>G	ENSP00000433191.1:p.Arg144Gly
ENST00000527953.5:n.685C>G
ENST00000533320.5:n.664C>G
ENST00000535898.5:c.124C>G	ENSP00000445062.1:p.Arg42Gly
ENST00000539050.5:c.220C>G	ENSP00000442343.2:p.Arg74Gly
ENST00000623108.3:c.220C>G	ENSP00000485110.1:p.Arg74Gly
ENST00000628935.1:c.172C>G	ENSP00000487145.1:p.Arg58Gly
NM_000770.3:c.430C>G MANE Select	NP_000761.3:p.Arg144Gly
NM_001198853.1:c.220C>G	NP_001185782.1:p.Arg74Gly
NM_001198854.1:c.124C>G	NP_001185783.1:p.Arg42Gly
NM_001198855.1:c.220C>G	NP_001185784.1:p.Arg74Gly
XR_945610.1:n.526C>G