Canonical Allele Identifier: CA377682654

Gene: CYP2C8

Linked Data

• dbSNP Id: rs1351974661
• gnomAD v2: 10-96826978-C-A
• gnomAD v4: 10-95067221-C-A
• MyVariant Identifiers: chr10:g.96826978C>A (hg19) ; chr10:g.95067221C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.95067221C>A , CM000672.2:g.95067221C>A	GRCh38
NC_000010.10:g.96826978C>A , CM000672.1:g.96826978C>A	GRCh37
NC_000010.9:g.96816968C>A	NCBI36
NG_007972.1:g.7277G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371270.6:c.468G>T MANE Select	ENSP00000360317.3:p.Leu156Phe
ENST00000371270.5:c.468G>T	ENSP00000360317.3:p.Leu156Phe
ENST00000479946.2:n.772G>T
ENST00000490994.6:c.*254G>T	ENSP00000433314.1:n.*254G>T
ENST00000525991.5:c.*43G>T	ENSP00000433842.1:n.*43G>T
ENST00000526814.5:n.723G>T
ENST00000527420.5:c.468G>T	ENSP00000433191.1:p.Leu156Phe
ENST00000527953.5:n.723G>T
ENST00000533320.5:n.702G>T
ENST00000535898.5:c.162G>T	ENSP00000445062.1:p.Leu54Phe
ENST00000539050.5:c.258G>T	ENSP00000442343.2:p.Leu86Phe
ENST00000623108.3:c.258G>T	ENSP00000485110.1:p.Leu86Phe
ENST00000628935.1:c.210G>T	ENSP00000487145.1:p.Leu70Phe
NM_000770.3:c.468G>T MANE Select	NP_000761.3:p.Leu156Phe
NM_001198853.1:c.258G>T	NP_001185782.1:p.Leu86Phe
NM_001198854.1:c.162G>T	NP_001185783.1:p.Leu54Phe
NM_001198855.1:c.258G>T	NP_001185784.1:p.Leu86Phe
XR_945610.1:n.564G>T