Canonical Allele Identifier: CA377677285

Gene: CYP2C8

Linked Data

• dbSNP Id: rs757657903
• gnomAD v3: 10-95037154-A-G
• gnomAD v4: 10-95037154-A-G
• MyVariant Identifiers: chr10:g.96796911A>G (hg19) ; chr10:g.95037154A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.95037154A>G , CM000672.2:g.95037154A>G	GRCh38
NC_000010.10:g.96796911A>G , CM000672.1:g.96796911A>G	GRCh37
NC_000010.9:g.96786901A>G	NCBI36
NG_007972.1:g.37344T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371270.6:c.1447T>C MANE Select	ENSP00000360317.3:p.Tyr483His
ENST00000371270.5:c.1447T>C	ENSP00000360317.3:p.Tyr483His
ENST00000490994.6:c.*1233T>C	ENSP00000433314.1:n.*1233T>C
ENST00000525991.5:c.*1022T>C	ENSP00000433842.1:n.*1022T>C
ENST00000526814.5:n.1702T>C
ENST00000527420.5:c.*304T>C	ENSP00000433191.1:n.*304T>C
ENST00000527953.5:n.1741T>C
ENST00000533320.5:n.1681T>C
ENST00000535898.5:c.1141T>C	ENSP00000445062.1:p.Tyr381His
ENST00000539050.5:c.1237T>C	ENSP00000442343.2:p.Tyr413His
ENST00000623108.3:c.1237T>C	ENSP00000485110.1:p.Tyr413His
NM_000770.3:c.1447T>C MANE Select	NP_000761.3:p.Tyr483His
NM_001198853.1:c.1237T>C	NP_001185782.1:p.Tyr413His
NM_001198854.1:c.1141T>C	NP_001185783.1:p.Tyr381His
NM_001198855.1:c.1237T>C	NP_001185784.1:p.Tyr413His