Canonical Allele Identifier: CA377683347

Gene: CYP2C8

Linked Data

• MyVariant Identifiers: chr10:g.96827121A>C (hg19) ; chr10:g.95067364A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.95067364A>C , CM000672.2:g.95067364A>C	GRCh38
NC_000010.10:g.96827121A>C , CM000672.1:g.96827121A>C	GRCh37
NC_000010.9:g.96817111A>C	NCBI36
NG_007972.1:g.7134T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371270.6:c.332-7T>G MANE Select	ENSP00000360317.3:n.332-7T>G
ENST00000371270.5:c.332-7T>G	ENSP00000360317.3:n.332-7T>G
ENST00000479946.2:n.629T>G
ENST00000490994.6:c.*118-7T>G	ENSP00000433314.1:n.*118-7T>G
ENST00000525991.5:c.207-7T>G	ENSP00000433842.1:n.207-7T>G
ENST00000526814.5:n.580T>G
ENST00000527420.5:c.332-7T>G	ENSP00000433191.1:n.332-7T>G
ENST00000527953.5:n.580T>G
ENST00000533320.5:n.559T>G
ENST00000535898.5:c.26-7T>G	ENSP00000445062.1:n.26-7T>G
ENST00000539050.5:c.122-7T>G	ENSP00000442343.2:n.122-7T>G
ENST00000623108.3:c.122-7T>G	ENSP00000485110.1:n.122-7T>G
ENST00000628935.1:c.67T>G	ENSP00000487145.1:p.Leu23Val
NM_000770.3:c.332-7T>G MANE Select	NP_000761.3:n.332-7T>G
NM_001198853.1:c.122-7T>G	NP_001185782.1:n.122-7T>G
NM_001198854.1:c.26-7T>G	NP_001185783.1:n.26-7T>G
NM_001198855.1:c.122-7T>G	NP_001185784.1:n.122-7T>G
XR_945610.1:n.428-7T>G