Canonical Allele Identifier: CA377682645

Gene: CYP2C8

Linked Data

• gnomAD v4: 10-95067219-C-G
• MyVariant Identifiers: chr10:g.96826976C>G (hg19) ; chr10:g.95067219C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.95067219C>G , CM000672.2:g.95067219C>G	GRCh38
NC_000010.10:g.96826976C>G , CM000672.1:g.96826976C>G	GRCh37
NC_000010.9:g.96816966C>G	NCBI36
NG_007972.1:g.7279G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371270.6:c.470G>C MANE Select	ENSP00000360317.3:p.Arg157Thr
ENST00000371270.5:c.470G>C	ENSP00000360317.3:p.Arg157Thr
ENST00000479946.2:n.774G>C
ENST00000490994.6:c.*256G>C	ENSP00000433314.1:n.*256G>C
ENST00000525991.5:c.*45G>C	ENSP00000433842.1:n.*45G>C
ENST00000526814.5:n.725G>C
ENST00000527420.5:c.470G>C	ENSP00000433191.1:p.Arg157Thr
ENST00000527953.5:n.725G>C
ENST00000533320.5:n.704G>C
ENST00000535898.5:c.164G>C	ENSP00000445062.1:p.Arg55Thr
ENST00000539050.5:c.260G>C	ENSP00000442343.2:p.Arg87Thr
ENST00000623108.3:c.260G>C	ENSP00000485110.1:p.Arg87Thr
ENST00000628935.1:c.212G>C	ENSP00000487145.1:p.Arg71Thr
NM_000770.3:c.470G>C MANE Select	NP_000761.3:p.Arg157Thr
NM_001198853.1:c.260G>C	NP_001185782.1:p.Arg87Thr
NM_001198854.1:c.164G>C	NP_001185783.1:p.Arg55Thr
NM_001198855.1:c.260G>C	NP_001185784.1:p.Arg87Thr
XR_945610.1:n.566G>C