Canonical Allele Identifier: CA377683005

Gene: CYP2C8

Linked Data

• dbSNP Id: rs1180517714
• gnomAD v2: 10-96827038-C-T
• gnomAD v3: 10-95067281-C-T
• gnomAD v4: 10-95067281-C-T
• MyVariant Identifiers: chr10:g.96827038C>T (hg19) ; chr10:g.95067281C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.95067281C>T , CM000672.2:g.95067281C>T	GRCh38
NC_000010.10:g.96827038C>T , CM000672.1:g.96827038C>T	GRCh37
NC_000010.9:g.96817028C>T	NCBI36
NG_007972.1:g.7217G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000371270.6:c.408G>A MANE Select	ENSP00000360317.3:p.Met136Ile
ENST00000371270.5:c.408G>A	ENSP00000360317.3:p.Met136Ile
ENST00000479946.2:n.712G>A
ENST00000490994.6:c.*194G>A	ENSP00000433314.1:n.*194G>A
ENST00000525991.5:c.283G>A	ENSP00000433842.1:p.Gly95Arg
ENST00000526814.5:n.663G>A
ENST00000527420.5:c.408G>A	ENSP00000433191.1:p.Met136Ile
ENST00000527953.5:n.663G>A
ENST00000533320.5:n.642G>A
ENST00000535898.5:c.102G>A	ENSP00000445062.1:p.Met34Ile
ENST00000539050.5:c.198G>A	ENSP00000442343.2:p.Met66Ile
ENST00000623108.3:c.198G>A	ENSP00000485110.1:p.Met66Ile
ENST00000628935.1:c.150G>A	ENSP00000487145.1:p.Met50Ile
NM_000770.3:c.408G>A MANE Select	NP_000761.3:p.Met136Ile
NM_001198853.1:c.198G>A	NP_001185782.1:p.Met66Ile
NM_001198854.1:c.102G>A	NP_001185783.1:p.Met34Ile
NM_001198855.1:c.198G>A	NP_001185784.1:p.Met66Ile
XR_945610.1:n.504G>A