Canonical Allele Identifier: CA1929359345

Gene: CYP2C8

Linked Data

• dbSNP Id: rs1564733642

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.95040988A>G , CM000672.2:g.95040988A>G	GRCh38
NC_000010.10:g.96800745A>G , CM000672.1:g.96800745A>G	GRCh37
NC_000010.9:g.96790735A>G	NCBI36
NG_007972.1:g.33510T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371270.6:c.1149+1902T>C MANE Select	ENSP00000360317.3:n.1149+1902T>C
ENST00000371270.5:c.1149+1902T>C	ENSP00000360317.3:n.1149+1902T>C
ENST00000479946.2:n.1454-28T>C
ENST00000490994.6:c.*935+1902T>C	ENSP00000433314.1:n.*935+1902T>C
ENST00000525991.5:c.*724+1902T>C	ENSP00000433842.1:n.*724+1902T>C
ENST00000526814.5:n.1404+1902T>C
ENST00000527420.5:c.1150-28T>C	ENSP00000433191.1:n.1150-28T>C
ENST00000527953.5:n.1405-28T>C
ENST00000533320.5:n.1383+1902T>C
ENST00000535898.5:c.843+1902T>C	ENSP00000445062.1:n.843+1902T>C
ENST00000539050.5:c.939+1902T>C	ENSP00000442343.2:n.939+1902T>C
ENST00000623108.3:c.939+1902T>C	ENSP00000485110.1:n.939+1902T>C
ENST00000628935.1:c.892-28T>C	ENSP00000487145.1:n.892-28T>C
NM_000770.3:c.1149+1902T>C MANE Select	NP_000761.3:n.1149+1902T>C
NM_001198853.1:c.939+1902T>C	NP_001185782.1:n.939+1902T>C
NM_001198854.1:c.843+1902T>C	NP_001185783.1:n.843+1902T>C
NM_001198855.1:c.939+1902T>C	NP_001185784.1:n.939+1902T>C
XR_945610.1:n.1246-28T>C