Canonical Allele Identifier: CA5617455

Gene: CYP2C8

Linked Data

• dbSNP Id: rs762359438
• ExAC: 10:96796877 A / G
• gnomAD v2: 10-96796877-A-G
• gnomAD v4: 10-95037120-A-G
• MyVariant Identifiers: chr10:g.96796877A>G (hg19) ; chr10:g.95037120A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.95037120A>G , CM000672.2:g.95037120A>G	GRCh38
NC_000010.10:g.96796877A>G , CM000672.1:g.96796877A>G	GRCh37
NC_000010.9:g.96786867A>G	NCBI36
NG_007972.1:g.37378T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371270.6:c.*8T>C MANE Select	ENSP00000360317.3:n.*8T>C
ENST00000371270.5:c.*8T>C	ENSP00000360317.3:n.*8T>C
ENST00000490994.6:c.*1267T>C	ENSP00000433314.1:n.*1267T>C
ENST00000525991.5:c.*1056T>C	ENSP00000433842.1:n.*1056T>C
ENST00000526814.5:n.1736T>C
ENST00000527420.5:c.*338T>C	ENSP00000433191.1:n.*338T>C
ENST00000527953.5:n.1775T>C
ENST00000533320.5:n.1715T>C
ENST00000535898.5:c.*8T>C	ENSP00000445062.1:n.*8T>C
ENST00000539050.5:c.*8T>C	ENSP00000442343.2:n.*8T>C
ENST00000623108.3:c.*8T>C	ENSP00000485110.1:n.*8T>C
NM_000770.3:c.*8T>C MANE Select	NP_000761.3:n.*8T>C
NM_001198853.1:c.*8T>C	NP_001185782.1:n.*8T>C
NM_001198854.1:c.*8T>C	NP_001185783.1:n.*8T>C
NM_001198855.1:c.*8T>C	NP_001185784.1:n.*8T>C