Canonical Allele Identifier: CA931389205

Gene: CYP2C8

Linked Data

• dbSNP Id: rs2032913041
• gnomAD v3: 10-95037630-C-G
• gnomAD v4: 10-95037630-C-G

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.95037630C>G , CM000672.2:g.95037630C>G	GRCh38
NC_000010.10:g.96797387C>G , CM000672.1:g.96797387C>G	GRCh37
NC_000010.9:g.96787377C>G	NCBI36
NG_007972.1:g.36868G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000371270.6:c.1292-321G>C MANE Select	ENSP00000360317.3:n.1292-321G>C
ENST00000371270.5:c.1292-321G>C	ENSP00000360317.3:n.1292-321G>C
ENST00000490994.6:c.*1078-321G>C	ENSP00000433314.1:n.*1078-321G>C
ENST00000525991.5:c.*867-321G>C	ENSP00000433842.1:n.*867-321G>C
ENST00000526814.5:n.1547-321G>C
ENST00000527420.5:c.*149-321G>C	ENSP00000433191.1:n.*149-321G>C
ENST00000527953.5:n.1586-321G>C
ENST00000531714.1:n.480-321G>C
ENST00000533320.5:n.1526-321G>C
ENST00000535898.5:c.986-321G>C	ENSP00000445062.1:n.986-321G>C
ENST00000539050.5:c.1082-321G>C	ENSP00000442343.2:n.1082-321G>C
ENST00000623108.3:c.1082-321G>C	ENSP00000485110.1:n.1082-321G>C
NM_000770.3:c.1292-321G>C MANE Select	NP_000761.3:n.1292-321G>C
NM_001198853.1:c.1082-321G>C	NP_001185782.1:n.1082-321G>C
NM_001198854.1:c.986-321G>C	NP_001185783.1:n.986-321G>C
NM_001198855.1:c.1082-321G>C	NP_001185784.1:n.1082-321G>C
XR_945610.1:n.1427-321G>C