Canonical Allele Identifier: CA5617787

Gene: CYP2C8

Linked Data

• dbSNP Id: rs767098538
• ExAC: 10:96826986 C / T
• gnomAD v2: 10-96826986-C-T
• gnomAD v3: 10-95067229-C-T
• gnomAD v4: 10-95067229-C-T
• MyVariant Identifiers: chr10:g.96826986C>T (hg19) ; chr10:g.95067229C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.95067229C>T , CM000672.2:g.95067229C>T	GRCh38
NC_000010.10:g.96826986C>T , CM000672.1:g.96826986C>T	GRCh37
NC_000010.9:g.96816976C>T	NCBI36
NG_007972.1:g.7269G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371270.6:c.460G>A MANE Select	ENSP00000360317.3:p.Glu154Lys
ENST00000371270.5:c.460G>A	ENSP00000360317.3:p.Glu154Lys
ENST00000479946.2:n.764G>A
ENST00000490994.6:c.*246G>A	ENSP00000433314.1:n.*246G>A
ENST00000525991.5:c.*35G>A	ENSP00000433842.1:n.*35G>A
ENST00000526814.5:n.715G>A
ENST00000527420.5:c.460G>A	ENSP00000433191.1:p.Glu154Lys
ENST00000527953.5:n.715G>A
ENST00000533320.5:n.694G>A
ENST00000535898.5:c.154G>A	ENSP00000445062.1:p.Glu52Lys
ENST00000539050.5:c.250G>A	ENSP00000442343.2:p.Glu84Lys
ENST00000623108.3:c.250G>A	ENSP00000485110.1:p.Glu84Lys
ENST00000628935.1:c.202G>A	ENSP00000487145.1:p.Glu68Lys
NM_000770.3:c.460G>A MANE Select	NP_000761.3:p.Glu154Lys
NM_001198853.1:c.250G>A	NP_001185782.1:p.Glu84Lys
NM_001198854.1:c.154G>A	NP_001185783.1:p.Glu52Lys
NM_001198855.1:c.250G>A	NP_001185784.1:p.Glu84Lys
XR_945610.1:n.556G>A