Canonical Allele Identifier: CA5617481

Gene: CYP2C8

Linked Data

• dbSNP Id: rs754390283
• ExAC: 10:96797025 G / A
• gnomAD v2: 10-96797025-G-A
• gnomAD v3: 10-95037268-G-A
• gnomAD v4: 10-95037268-G-A
• MyVariant Identifiers: chr10:g.96797025G>A (hg19) ; chr10:g.95037268G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.95037268G>A , CM000672.2:g.95037268G>A	GRCh38
NC_000010.10:g.96797025G>A , CM000672.1:g.96797025G>A	GRCh37
NC_000010.9:g.96787015G>A	NCBI36
NG_007972.1:g.37230C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371270.6:c.1333C>T MANE Select	ENSP00000360317.3:p.Leu445=
ENST00000371270.5:c.1333C>T	ENSP00000360317.3:p.Leu445=
ENST00000490994.6:c.*1119C>T	ENSP00000433314.1:n.*1119C>T
ENST00000525991.5:c.*908C>T	ENSP00000433842.1:n.*908C>T
ENST00000526814.5:n.1588C>T
ENST00000527420.5:c.*190C>T	ENSP00000433191.1:n.*190C>T
ENST00000527953.5:n.1627C>T
ENST00000531714.1:n.521C>T
ENST00000533320.5:n.1567C>T
ENST00000535898.5:c.1027C>T	ENSP00000445062.1:p.Leu343=
ENST00000539050.5:c.1123C>T	ENSP00000442343.2:p.Leu375=
ENST00000623108.3:c.1123C>T	ENSP00000485110.1:p.Leu375=
NM_000770.3:c.1333C>T MANE Select	NP_000761.3:p.Leu445=
NM_001198853.1:c.1123C>T	NP_001185782.1:p.Leu375=
NM_001198854.1:c.1027C>T	NP_001185783.1:p.Leu343=
NM_001198855.1:c.1123C>T	NP_001185784.1:p.Leu375=
XR_945610.1:n.1468C>T