Canonical Allele Identifier: CA670224341

Gene: CYP2C8

Linked Data

• dbSNP Id: rs1461584997
• gnomAD v3: 10-95037099-A-C
• gnomAD v4: 10-95037099-A-C
• MyVariant Identifiers: chr10:g.96796856A>C (hg19) ; chr10:g.95037099A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.95037099A>C , CM000672.2:g.95037099A>C	GRCh38
NC_000010.10:g.96796856A>C , CM000672.1:g.96796856A>C	GRCh37
NC_000010.9:g.96786846A>C	NCBI36
NG_007972.1:g.37399T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371270.6:c.*29T>G MANE Select	ENSP00000360317.3:n.*29T>G
ENST00000371270.5:c.*29T>G	ENSP00000360317.3:n.*29T>G
ENST00000490994.6:c.*1288T>G	ENSP00000433314.1:n.*1288T>G
ENST00000525991.5:c.*1077T>G	ENSP00000433842.1:n.*1077T>G
ENST00000526814.5:n.1757T>G
ENST00000527420.5:c.*359T>G	ENSP00000433191.1:n.*359T>G
ENST00000527953.5:n.1796T>G
ENST00000533320.5:n.1736T>G
ENST00000535898.5:c.*29T>G	ENSP00000445062.1:n.*29T>G
ENST00000539050.5:c.*29T>G	ENSP00000442343.2:n.*29T>G
ENST00000623108.3:c.*29T>G	ENSP00000485110.1:n.*29T>G
NM_000770.3:c.*29T>G MANE Select	NP_000761.3:n.*29T>G
NM_001198853.1:c.*29T>G	NP_001185782.1:n.*29T>G
NM_001198854.1:c.*29T>G	NP_001185783.1:n.*29T>G
NM_001198855.1:c.*29T>G	NP_001185784.1:n.*29T>G