Canonical Allele Identifier: CA5617509

Gene: CYP2C8

Linked Data

• dbSNP Id: rs752621676
• ExAC: 10:96798665 G / T
• gnomAD v2: 10-96798665-G-T
• gnomAD v4: 10-95038908-G-T
• MyVariant Identifiers: chr10:g.96798665G>T (hg19) ; chr10:g.95038908G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.95038908G>T , CM000672.2:g.95038908G>T	GRCh38
NC_000010.10:g.96798665G>T , CM000672.1:g.96798665G>T	GRCh37
NC_000010.9:g.96788655G>T	NCBI36
NG_007972.1:g.35590C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000371270.6:c.1280C>A MANE Select	ENSP00000360317.3:p.Pro427His
ENST00000371270.5:c.1280C>A	ENSP00000360317.3:p.Pro427His
ENST00000490994.6:c.*1066C>A	ENSP00000433314.1:n.*1066C>A
ENST00000525991.5:c.*855C>A	ENSP00000433842.1:n.*855C>A
ENST00000526814.5:n.1535C>A
ENST00000527420.5:c.*137C>A	ENSP00000433191.1:n.*137C>A
ENST00000527953.5:n.1574C>A
ENST00000531714.1:n.468C>A
ENST00000533320.5:n.1514C>A
ENST00000535898.5:c.974C>A	ENSP00000445062.1:p.Pro325His
ENST00000539050.5:c.1070C>A	ENSP00000442343.2:p.Pro357His
ENST00000623108.3:c.1070C>A	ENSP00000485110.1:p.Pro357His
NM_000770.3:c.1280C>A MANE Select	NP_000761.3:p.Pro427His
NM_001198853.1:c.1070C>A	NP_001185782.1:p.Pro357His
NM_001198854.1:c.974C>A	NP_001185783.1:p.Pro325His
NM_001198855.1:c.1070C>A	NP_001185784.1:p.Pro357His
XR_945610.1:n.1415C>A