Canonical Allele Identifier: CA377683011

Gene: CYP2C8

Linked Data

• gnomAD v4: 10-95067282-A-G
• MyVariant Identifiers: chr10:g.96827039A>G (hg19) ; chr10:g.95067282A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.95067282A>G , CM000672.2:g.95067282A>G	GRCh38
NC_000010.10:g.96827039A>G , CM000672.1:g.96827039A>G	GRCh37
NC_000010.9:g.96817029A>G	NCBI36
NG_007972.1:g.7216T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000371270.6:c.407T>C MANE Select	ENSP00000360317.3:p.Met136Thr
ENST00000371270.5:c.407T>C	ENSP00000360317.3:p.Met136Thr
ENST00000479946.2:n.711T>C
ENST00000490994.6:c.*193T>C	ENSP00000433314.1:n.*193T>C
ENST00000525991.5:c.282T>C	ENSP00000433842.1:p.Asp94=
ENST00000526814.5:n.662T>C
ENST00000527420.5:c.407T>C	ENSP00000433191.1:p.Met136Thr
ENST00000527953.5:n.662T>C
ENST00000533320.5:n.641T>C
ENST00000535898.5:c.101T>C	ENSP00000445062.1:p.Met34Thr
ENST00000539050.5:c.197T>C	ENSP00000442343.2:p.Met66Thr
ENST00000623108.3:c.197T>C	ENSP00000485110.1:p.Met66Thr
ENST00000628935.1:c.149T>C	ENSP00000487145.1:p.Met50Thr
NM_000770.3:c.407T>C MANE Select	NP_000761.3:p.Met136Thr
NM_001198853.1:c.197T>C	NP_001185782.1:p.Met66Thr
NM_001198854.1:c.101T>C	NP_001185783.1:p.Met34Thr
NM_001198855.1:c.197T>C	NP_001185784.1:p.Met66Thr
XR_945610.1:n.503T>C