Canonical Allele Identifier: CA595332697

Gene: CYP2C8

Linked Data

• dbSNP Id: rs1323573679
• gnomAD v2: 10-96796830-A-T
• gnomAD v3: 10-95037073-A-T
• gnomAD v4: 10-95037073-A-T
• MyVariant Identifiers: chr10:g.96796830A>T (hg19) ; chr10:g.95037073A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.95037073A>T , CM000672.2:g.95037073A>T	GRCh38
NC_000010.10:g.96796830A>T , CM000672.1:g.96796830A>T	GRCh37
NC_000010.9:g.96786820A>T	NCBI36
NG_007972.1:g.37425T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371270.6:c.*55T>A MANE Select	ENSP00000360317.3:n.*55T>A
ENST00000371270.5:c.*55T>A	ENSP00000360317.3:n.*55T>A
ENST00000490994.6:c.*1314T>A	ENSP00000433314.1:n.*1314T>A
ENST00000525991.5:c.*1103T>A	ENSP00000433842.1:n.*1103T>A
ENST00000526814.5:n.1783T>A
ENST00000527420.5:c.*385T>A	ENSP00000433191.1:n.*385T>A
ENST00000527953.5:n.1822T>A
ENST00000533320.5:n.1762T>A
ENST00000535898.5:c.*55T>A	ENSP00000445062.1:n.*55T>A
ENST00000539050.5:c.*55T>A	ENSP00000442343.2:n.*55T>A
ENST00000623108.3:c.*55T>A	ENSP00000485110.1:n.*55T>A
NM_000770.3:c.*55T>A MANE Select	NP_000761.3:n.*55T>A
NM_001198853.1:c.*55T>A	NP_001185782.1:n.*55T>A
NM_001198854.1:c.*55T>A	NP_001185783.1:n.*55T>A
NM_001198855.1:c.*55T>A	NP_001185784.1:n.*55T>A