Canonical Allele Identifier: CA377677279

Gene: CYP2C8

Linked Data

• dbSNP Id: rs764390443
• gnomAD v3: 10-95037151-G-C
• gnomAD v4: 10-95037151-G-C
• MyVariant Identifiers: chr10:g.96796908G>C (hg19) ; chr10:g.95037151G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.95037151G>C , CM000672.2:g.95037151G>C	GRCh38
NC_000010.10:g.96796908G>C , CM000672.1:g.96796908G>C	GRCh37
NC_000010.9:g.96786898G>C	NCBI36
NG_007972.1:g.37347C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371270.6:c.1450C>G MANE Select	ENSP00000360317.3:p.Gln484Glu
ENST00000371270.5:c.1450C>G	ENSP00000360317.3:p.Gln484Glu
ENST00000490994.6:c.*1236C>G	ENSP00000433314.1:n.*1236C>G
ENST00000525991.5:c.*1025C>G	ENSP00000433842.1:n.*1025C>G
ENST00000526814.5:n.1705C>G
ENST00000527420.5:c.*307C>G	ENSP00000433191.1:n.*307C>G
ENST00000527953.5:n.1744C>G
ENST00000533320.5:n.1684C>G
ENST00000535898.5:c.1144C>G	ENSP00000445062.1:p.Gln382Glu
ENST00000539050.5:c.1240C>G	ENSP00000442343.2:p.Gln414Glu
ENST00000623108.3:c.1240C>G	ENSP00000485110.1:p.Gln414Glu
NM_000770.3:c.1450C>G MANE Select	NP_000761.3:p.Gln484Glu
NM_001198853.1:c.1240C>G	NP_001185782.1:p.Gln414Glu
NM_001198854.1:c.1144C>G	NP_001185783.1:p.Gln382Glu
NM_001198855.1:c.1240C>G	NP_001185784.1:p.Gln414Glu