Canonical Allele Identifier: CA470841240

Gene: CYP2C8

Linked Data

• MyVariant Identifiers: chr10:g.96797047T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.95037290T>C , CM000672.2:g.95037290T>C	GRCh38
NC_000010.10:g.96797047T>C , CM000672.1:g.96797047T>C	GRCh37
NC_000010.9:g.96787037T>C	NCBI36
NG_007972.1:g.37208A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371270.6:c.1311A>G MANE Select	ENSP00000360317.3:p.Gly437=
ENST00000371270.5:c.1311A>G	ENSP00000360317.3:p.Gly437=
ENST00000490994.6:c.*1097A>G	ENSP00000433314.1:n.*1097A>G
ENST00000525991.5:c.*886A>G	ENSP00000433842.1:n.*886A>G
ENST00000526814.5:n.1566A>G
ENST00000527420.5:c.*168A>G	ENSP00000433191.1:n.*168A>G
ENST00000527953.5:n.1605A>G
ENST00000531714.1:n.499A>G
ENST00000533320.5:n.1545A>G
ENST00000535898.5:c.1005A>G	ENSP00000445062.1:p.Gly335=
ENST00000539050.5:c.1101A>G	ENSP00000442343.2:p.Gly367=
ENST00000623108.3:c.1101A>G	ENSP00000485110.1:p.Gly367=
NM_000770.3:c.1311A>G MANE Select	NP_000761.3:p.Gly437=
NM_001198853.1:c.1101A>G	NP_001185782.1:p.Gly367=
NM_001198854.1:c.1005A>G	NP_001185783.1:p.Gly335=
NM_001198855.1:c.1101A>G	NP_001185784.1:p.Gly367=
XR_945610.1:n.1446A>G