Canonical Allele Identifier: CA211730721

Gene: CYP2C8

Linked Data

• dbSNP Id: rs201739495
• gnomAD v3: 10-95067321-A-T
• gnomAD v4: 10-95067321-A-T
• MyVariant Identifiers: chr10:g.96827078A>T (hg19) ; chr10:g.95067321A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.95067321A>T , CM000672.2:g.95067321A>T	GRCh38
NC_000010.10:g.96827078A>T , CM000672.1:g.96827078A>T	GRCh37
NC_000010.9:g.96817068A>T	NCBI36
NG_007972.1:g.7177T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371270.6:c.368T>A MANE Select	ENSP00000360317.3:p.Ile123Asn
ENST00000371270.5:c.368T>A	ENSP00000360317.3:p.Ile123Asn
ENST00000479946.2:n.672T>A
ENST00000490994.6:c.*154T>A	ENSP00000433314.1:n.*154T>A
ENST00000525991.5:c.243T>A	ENSP00000433842.1:p.Asp81Glu
ENST00000526814.5:n.623T>A
ENST00000527420.5:c.368T>A	ENSP00000433191.1:p.Ile123Asn
ENST00000527953.5:n.623T>A
ENST00000533320.5:n.602T>A
ENST00000535898.5:c.62T>A	ENSP00000445062.1:p.Ile21Asn
ENST00000539050.5:c.158T>A	ENSP00000442343.2:p.Ile53Asn
ENST00000623108.3:c.158T>A	ENSP00000485110.1:p.Ile53Asn
ENST00000628935.1:c.110T>A	ENSP00000487145.1:p.Ile37Asn
NM_000770.3:c.368T>A MANE Select	NP_000761.3:p.Ile123Asn
NM_001198853.1:c.158T>A	NP_001185782.1:p.Ile53Asn
NM_001198854.1:c.62T>A	NP_001185783.1:p.Ile21Asn
NM_001198855.1:c.158T>A	NP_001185784.1:p.Ile53Asn
XR_945610.1:n.464T>A