Canonical Allele Identifier: CA595332710

Gene: CYP2C8

Linked Data

• dbSNP Id: rs1564732241
• gnomAD v2: 10-96796846-A-G
• gnomAD v4: 10-95037089-A-G
• MyVariant Identifiers: chr10:g.96796846_96796860delinsGGGTGATAGCAGATC (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.95037089A>G , CM000672.2:g.95037089A>G	GRCh38
NC_000010.10:g.96796846A>G , CM000672.1:g.96796846A>G	GRCh37
NC_000010.9:g.96786836A>G	NCBI36
NG_007972.1:g.37409T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371270.6:c.*39T>C MANE Select	ENSP00000360317.3:n.*39T>C
ENST00000371270.5:c.*39T>C	ENSP00000360317.3:n.*39T>C
ENST00000490994.6:c.*1298T>C	ENSP00000433314.1:n.*1298T>C
ENST00000525991.5:c.*1087T>C	ENSP00000433842.1:n.*1087T>C
ENST00000526814.5:n.1767T>C
ENST00000527420.5:c.*369T>C	ENSP00000433191.1:n.*369T>C
ENST00000527953.5:n.1806T>C
ENST00000533320.5:n.1746T>C
ENST00000535898.5:c.*39T>C	ENSP00000445062.1:n.*39T>C
ENST00000539050.5:c.*39T>C	ENSP00000442343.2:n.*39T>C
ENST00000623108.3:c.*39T>C	ENSP00000485110.1:n.*39T>C
NM_000770.3:c.*39T>C MANE Select	NP_000761.3:n.*39T>C
NM_001198853.1:c.*39T>C	NP_001185782.1:n.*39T>C
NM_001198854.1:c.*39T>C	NP_001185783.1:n.*39T>C
NM_001198855.1:c.*39T>C	NP_001185784.1:n.*39T>C