Canonical Allele Identifier: CA5617471

Gene: CYP2C8

Linked Data

• dbSNP Id: rs769773346
• ExAC: 10:96796962 T / A
• gnomAD v2: 10-96796962-T-A
• gnomAD v4: 10-95037205-T-A
• MyVariant Identifiers: chr10:g.96796962T>A (hg19) ; chr10:g.95037205T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.95037205T>A , CM000672.2:g.95037205T>A	GRCh38
NC_000010.10:g.96796962T>A , CM000672.1:g.96796962T>A	GRCh37
NC_000010.9:g.96786952T>A	NCBI36
NG_007972.1:g.37293A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371270.6:c.1396A>T MANE Select	ENSP00000360317.3:p.Asn466Tyr
ENST00000371270.5:c.1396A>T	ENSP00000360317.3:p.Asn466Tyr
ENST00000490994.6:c.*1182A>T	ENSP00000433314.1:n.*1182A>T
ENST00000525991.5:c.*971A>T	ENSP00000433842.1:n.*971A>T
ENST00000526814.5:n.1651A>T
ENST00000527420.5:c.*253A>T	ENSP00000433191.1:n.*253A>T
ENST00000527953.5:n.1690A>T
ENST00000531714.1:n.584A>T
ENST00000533320.5:n.1630A>T
ENST00000535898.5:c.1090A>T	ENSP00000445062.1:p.Asn364Tyr
ENST00000539050.5:c.1186A>T	ENSP00000442343.2:p.Asn396Tyr
ENST00000623108.3:c.1186A>T	ENSP00000485110.1:p.Asn396Tyr
NM_000770.3:c.1396A>T MANE Select	NP_000761.3:p.Asn466Tyr
NM_001198853.1:c.1186A>T	NP_001185782.1:p.Asn396Tyr
NM_001198854.1:c.1090A>T	NP_001185783.1:p.Asn364Tyr
NM_001198855.1:c.1186A>T	NP_001185784.1:p.Asn396Tyr
XR_945610.1:n.1531A>T