Canonical Allele Identifier: CA470841184

Gene: CYP2C8

Linked Data

• MyVariant Identifiers: chr10:g.96796954A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.95037197A>G , CM000672.2:g.95037197A>G	GRCh38
NC_000010.10:g.96796954A>G , CM000672.1:g.96796954A>G	GRCh37
NC_000010.9:g.96786944A>G	NCBI36
NG_007972.1:g.37301T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371270.6:c.1404T>C MANE Select	ENSP00000360317.3:p.Asn468=
ENST00000371270.5:c.1404T>C	ENSP00000360317.3:p.Asn468=
ENST00000490994.6:c.*1190T>C	ENSP00000433314.1:n.*1190T>C
ENST00000525991.5:c.*979T>C	ENSP00000433842.1:n.*979T>C
ENST00000526814.5:n.1659T>C
ENST00000527420.5:c.*261T>C	ENSP00000433191.1:n.*261T>C
ENST00000527953.5:n.1698T>C
ENST00000531714.1:n.592T>C
ENST00000533320.5:n.1638T>C
ENST00000535898.5:c.1098T>C	ENSP00000445062.1:p.Asn366=
ENST00000539050.5:c.1194T>C	ENSP00000442343.2:p.Asn398=
ENST00000623108.3:c.1194T>C	ENSP00000485110.1:p.Asn398=
NM_000770.3:c.1404T>C MANE Select	NP_000761.3:p.Asn468=
NM_001198853.1:c.1194T>C	NP_001185782.1:p.Asn398=
NM_001198854.1:c.1098T>C	NP_001185783.1:p.Asn366=
NM_001198855.1:c.1194T>C	NP_001185784.1:p.Asn398=
XR_945610.1:n.1539T>C