Canonical Allele Identifier: CA470841195

Gene: CYP2C8

Linked Data

• MyVariant Identifiers: chr10:g.96796975A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.95037218A>C , CM000672.2:g.95037218A>C	GRCh38
NC_000010.10:g.96796975A>C , CM000672.1:g.96796975A>C	GRCh37
NC_000010.9:g.96786965A>C	NCBI36
NG_007972.1:g.37280T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371270.6:c.1383T>G MANE Select	ENSP00000360317.3:p.Val461=
ENST00000371270.5:c.1383T>G	ENSP00000360317.3:p.Val461=
ENST00000490994.6:c.*1169T>G	ENSP00000433314.1:n.*1169T>G
ENST00000525991.5:c.*958T>G	ENSP00000433842.1:n.*958T>G
ENST00000526814.5:n.1638T>G
ENST00000527420.5:c.*240T>G	ENSP00000433191.1:n.*240T>G
ENST00000527953.5:n.1677T>G
ENST00000531714.1:n.571T>G
ENST00000533320.5:n.1617T>G
ENST00000535898.5:c.1077T>G	ENSP00000445062.1:p.Val359=
ENST00000539050.5:c.1173T>G	ENSP00000442343.2:p.Val391=
ENST00000623108.3:c.1173T>G	ENSP00000485110.1:p.Val391=
NM_000770.3:c.1383T>G MANE Select	NP_000761.3:p.Val461=
NM_001198853.1:c.1173T>G	NP_001185782.1:p.Val391=
NM_001198854.1:c.1077T>G	NP_001185783.1:p.Val359=
NM_001198855.1:c.1173T>G	NP_001185784.1:p.Val391=
XR_945610.1:n.1518T>G