Canonical Allele Identifier: CA5617452

Gene: CYP2C8

Linked Data

• dbSNP Id: rs371808080
• ExAC: 10:96796869 G / T
• gnomAD v2: 10-96796869-G-T
• gnomAD v4: 10-95037112-G-T
• MyVariant Identifiers: chr10:g.96796869G>T (hg19) ; chr10:g.95037112G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.95037112G>T , CM000672.2:g.95037112G>T	GRCh38
NC_000010.10:g.96796869G>T , CM000672.1:g.96796869G>T	GRCh37
NC_000010.9:g.96786859G>T	NCBI36
NG_007972.1:g.37386C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371270.6:c.*16C>A MANE Select	ENSP00000360317.3:n.*16C>A
ENST00000371270.5:c.*16C>A	ENSP00000360317.3:n.*16C>A
ENST00000490994.6:c.*1275C>A	ENSP00000433314.1:n.*1275C>A
ENST00000525991.5:c.*1064C>A	ENSP00000433842.1:n.*1064C>A
ENST00000526814.5:n.1744C>A
ENST00000527420.5:c.*346C>A	ENSP00000433191.1:n.*346C>A
ENST00000527953.5:n.1783C>A
ENST00000533320.5:n.1723C>A
ENST00000535898.5:c.*16C>A	ENSP00000445062.1:n.*16C>A
ENST00000539050.5:c.*16C>A	ENSP00000442343.2:n.*16C>A
ENST00000623108.3:c.*16C>A	ENSP00000485110.1:n.*16C>A
NM_000770.3:c.*16C>A MANE Select	NP_000761.3:n.*16C>A
NM_001198853.1:c.*16C>A	NP_001185782.1:n.*16C>A
NM_001198854.1:c.*16C>A	NP_001185783.1:n.*16C>A
NM_001198855.1:c.*16C>A	NP_001185784.1:n.*16C>A