Canonical Allele Identifier: CA5617527
Gene: CYP2C8 HGNC NCBI

Identifiers and link-outs to other resources

ClinVar Variation Id: 375654
ClinVar RCV Id: RCV000660764
dbSNP Id: rs10509681

User contributed link-outs

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.95038992T>C , CM000672.2:g.95038992T>C GRCh38
NC_000010.10:g.96798749T>C , CM000672.1:g.96798749T>C GRCh37
NC_000010.9:g.96788739T>C NCBI36
NG_007972.1:g.35506A>G

Transcript Alleles

HGVS Amino-acid change
NM_000770.3:c.1196A>G VV MANE Preferred NP_000761.3:p.Lys399Arg
NM_001198853.1:c.986A>G VV NP_001185782.1:p.Lys329Arg
NM_001198854.1:c.890A>G VV NP_001185783.1:p.Lys297Arg
NM_001198855.1:c.986A>G VV NP_001185784.1:p.Lys329Arg
XR_945610.1:n.1331A>G
ENST00000371270.5:c.1196A>G ENSP00000360317.3:p.Lys399Arg
ENST00000479946.2:n.1539A>G
ENST00000490994.6:c.*982A>G ENSP00000433314.1:p.=
ENST00000525991.5:c.*771A>G ENSP00000433842.1:p.=
ENST00000526814.5:n.1451A>G
ENST00000527420.5:c.*53A>G ENSP00000433191.1:p.=
ENST00000527953.5:n.1490A>G
ENST00000531714.1:n.384A>G
ENST00000533320.5:n.1430A>G
ENST00000535898.5:c.890A>G ENSP00000445062.1:p.Lys297Arg
ENST00000539050.5:c.986A>G ENSP00000442343.2:p.Lys329Arg
ENST00000623108.3:c.986A>G ENSP00000485110.1:p.Lys329Arg