Canonical Allele Identifier: CA377683250

Gene: CYP2C8

Linked Data

• MyVariant Identifiers: chr10:g.96827099T>G (hg19) ; chr10:g.95067342T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.95067342T>G , CM000672.2:g.95067342T>G	GRCh38
NC_000010.10:g.96827099T>G , CM000672.1:g.96827099T>G	GRCh37
NC_000010.9:g.96817089T>G	NCBI36
NG_007972.1:g.7156A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371270.6:c.347A>C MANE Select	ENSP00000360317.3:p.Asn116Thr
ENST00000371270.5:c.347A>C	ENSP00000360317.3:p.Asn116Thr
ENST00000479946.2:n.651A>C
ENST00000490994.6:c.*133A>C	ENSP00000433314.1:n.*133A>C
ENST00000525991.5:c.222A>C	ENSP00000433842.1:p.Gln74His
ENST00000526814.5:n.602A>C
ENST00000527420.5:c.347A>C	ENSP00000433191.1:p.Asn116Thr
ENST00000527953.5:n.602A>C
ENST00000533320.5:n.581A>C
ENST00000535898.5:c.41A>C	ENSP00000445062.1:p.Asn14Thr
ENST00000539050.5:c.137A>C	ENSP00000442343.2:p.Asn46Thr
ENST00000623108.3:c.137A>C	ENSP00000485110.1:p.Asn46Thr
ENST00000628935.1:c.89A>C	ENSP00000487145.1:p.Asn30Thr
NM_000770.3:c.347A>C MANE Select	NP_000761.3:p.Asn116Thr
NM_001198853.1:c.137A>C	NP_001185782.1:p.Asn46Thr
NM_001198854.1:c.41A>C	NP_001185783.1:p.Asn14Thr
NM_001198855.1:c.137A>C	NP_001185784.1:p.Asn46Thr
XR_945610.1:n.443A>C