Canonical Allele Identifier: CA377677262

Gene: CYP2C8

Linked Data

• dbSNP Id: rs1368648999
• gnomAD v2: 10-96796901-C-A
• gnomAD v4: 10-95037144-C-A
• MyVariant Identifiers: chr10:g.96796901C>A (hg19) ; chr10:g.95037144C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.95037144C>A , CM000672.2:g.95037144C>A	GRCh38
NC_000010.10:g.96796901C>A , CM000672.1:g.96796901C>A	GRCh37
NC_000010.9:g.96786891C>A	NCBI36
NG_007972.1:g.37354G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371270.6:c.1457G>T MANE Select	ENSP00000360317.3:p.Cys486Phe
ENST00000371270.5:c.1457G>T	ENSP00000360317.3:p.Cys486Phe
ENST00000490994.6:c.*1243G>T	ENSP00000433314.1:n.*1243G>T
ENST00000525991.5:c.*1032G>T	ENSP00000433842.1:n.*1032G>T
ENST00000526814.5:n.1712G>T
ENST00000527420.5:c.*314G>T	ENSP00000433191.1:n.*314G>T
ENST00000527953.5:n.1751G>T
ENST00000533320.5:n.1691G>T
ENST00000535898.5:c.1151G>T	ENSP00000445062.1:p.Cys384Phe
ENST00000539050.5:c.1247G>T	ENSP00000442343.2:p.Cys416Phe
ENST00000623108.3:c.1247G>T	ENSP00000485110.1:p.Cys416Phe
NM_000770.3:c.1457G>T MANE Select	NP_000761.3:p.Cys486Phe
NM_001198853.1:c.1247G>T	NP_001185782.1:p.Cys416Phe
NM_001198854.1:c.1151G>T	NP_001185783.1:p.Cys384Phe
NM_001198855.1:c.1247G>T	NP_001185784.1:p.Cys416Phe