Canonical Allele Identifier: CA211714377

Gene: CYP2C8

Linked Data

• dbSNP Id: rs193089188
• gnomAD v3: 10-95041134-T-G
• gnomAD v4: 10-95041134-T-G
• MyVariant Identifiers: chr10:g.96800891T>G (hg19) ; chr10:g.95041134T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.95041134T>G , CM000672.2:g.95041134T>G	GRCh38
NC_000010.10:g.96800891T>G , CM000672.1:g.96800891T>G	GRCh37
NC_000010.9:g.96790881T>G	NCBI36
NG_007972.1:g.33364A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000371270.6:c.1149+1756A>C MANE Select	ENSP00000360317.3:n.1149+1756A>C
ENST00000371270.5:c.1149+1756A>C	ENSP00000360317.3:n.1149+1756A>C
ENST00000479946.2:n.1454-174A>C
ENST00000490994.6:c.*935+1756A>C	ENSP00000433314.1:n.*935+1756A>C
ENST00000525991.5:c.*724+1756A>C	ENSP00000433842.1:n.*724+1756A>C
ENST00000526814.5:n.1404+1756A>C
ENST00000527420.5:c.1150-174A>C	ENSP00000433191.1:n.1150-174A>C
ENST00000527953.5:n.1405-174A>C
ENST00000533320.5:n.1383+1756A>C
ENST00000535898.5:c.843+1756A>C	ENSP00000445062.1:n.843+1756A>C
ENST00000539050.5:c.939+1756A>C	ENSP00000442343.2:n.939+1756A>C
ENST00000623108.3:c.939+1756A>C	ENSP00000485110.1:n.939+1756A>C
ENST00000628935.1:c.892-174A>C	ENSP00000487145.1:n.892-174A>C
NM_000770.3:c.1149+1756A>C MANE Select	NP_000761.3:n.1149+1756A>C
NM_001198853.1:c.939+1756A>C	NP_001185782.1:n.939+1756A>C
NM_001198854.1:c.843+1756A>C	NP_001185783.1:n.843+1756A>C
NM_001198855.1:c.939+1756A>C	NP_001185784.1:n.939+1756A>C
XR_945610.1:n.1246-174A>C