Canonical Allele Identifier: CA931388966

Gene: CYP2C8

Linked Data

• dbSNP Id: rs772241285
• gnomAD v3: 10-95037086-T-C
• gnomAD v4: 10-95037086-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.95037086T>C , CM000672.2:g.95037086T>C	GRCh38
NC_000010.10:g.96796843T>C , CM000672.1:g.96796843T>C	GRCh37
NC_000010.9:g.96786833T>C	NCBI36
NG_007972.1:g.37412A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371270.6:c.*42A>G MANE Select	ENSP00000360317.3:n.*42A>G
ENST00000371270.5:c.*42A>G	ENSP00000360317.3:n.*42A>G
ENST00000490994.6:c.*1301A>G	ENSP00000433314.1:n.*1301A>G
ENST00000525991.5:c.*1090A>G	ENSP00000433842.1:n.*1090A>G
ENST00000526814.5:n.1770A>G
ENST00000527420.5:c.*372A>G	ENSP00000433191.1:n.*372A>G
ENST00000527953.5:n.1809A>G
ENST00000533320.5:n.1749A>G
ENST00000535898.5:c.*42A>G	ENSP00000445062.1:n.*42A>G
ENST00000539050.5:c.*42A>G	ENSP00000442343.2:n.*42A>G
ENST00000623108.3:c.*42A>G	ENSP00000485110.1:n.*42A>G
NM_000770.3:c.*42A>G MANE Select	NP_000761.3:n.*42A>G
NM_001198853.1:c.*42A>G	NP_001185782.1:n.*42A>G
NM_001198854.1:c.*42A>G	NP_001185783.1:n.*42A>G
NM_001198855.1:c.*42A>G	NP_001185784.1:n.*42A>G