Canonical Allele Identifier: CA211711451

Gene: CYP2C8

Linked Data

• dbSNP Id: rs993994200
• gnomAD v4: 10-95037250-T-C
• MyVariant Identifiers: chr10:g.96797007T>C (hg19) ; chr10:g.95037250T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.95037250T>C , CM000672.2:g.95037250T>C	GRCh38
NC_000010.10:g.96797007T>C , CM000672.1:g.96797007T>C	GRCh37
NC_000010.9:g.96786997T>C	NCBI36
NG_007972.1:g.37248A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371270.6:c.1351A>G MANE Select	ENSP00000360317.3:p.Thr451Ala
ENST00000371270.5:c.1351A>G	ENSP00000360317.3:p.Thr451Ala
ENST00000490994.6:c.*1137A>G	ENSP00000433314.1:n.*1137A>G
ENST00000525991.5:c.*926A>G	ENSP00000433842.1:n.*926A>G
ENST00000526814.5:n.1606A>G
ENST00000527420.5:c.*208A>G	ENSP00000433191.1:n.*208A>G
ENST00000527953.5:n.1645A>G
ENST00000531714.1:n.539A>G
ENST00000533320.5:n.1585A>G
ENST00000535898.5:c.1045A>G	ENSP00000445062.1:p.Thr349Ala
ENST00000539050.5:c.1141A>G	ENSP00000442343.2:p.Thr381Ala
ENST00000623108.3:c.1141A>G	ENSP00000485110.1:p.Thr381Ala
NM_000770.3:c.1351A>G MANE Select	NP_000761.3:p.Thr451Ala
NM_001198853.1:c.1141A>G	NP_001185782.1:p.Thr381Ala
NM_001198854.1:c.1045A>G	NP_001185783.1:p.Thr349Ala
NM_001198855.1:c.1141A>G	NP_001185784.1:p.Thr381Ala
XR_945610.1:n.1486A>G