Canonical Allele Identifier: CA377677294

Gene: CYP2C8

Linked Data

• dbSNP Id: rs1371158132
• gnomAD v2: 10-96796916-G-T
• gnomAD v4: 10-95037159-G-T
• MyVariant Identifiers: chr10:g.96796916G>T (hg19) ; chr10:g.95037159G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.95037159G>T , CM000672.2:g.95037159G>T	GRCh38
NC_000010.10:g.96796916G>T , CM000672.1:g.96796916G>T	GRCh37
NC_000010.9:g.96786906G>T	NCBI36
NG_007972.1:g.37339C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371270.6:c.1442C>A MANE Select	ENSP00000360317.3:p.Pro481His
ENST00000371270.5:c.1442C>A	ENSP00000360317.3:p.Pro481His
ENST00000490994.6:c.*1228C>A	ENSP00000433314.1:n.*1228C>A
ENST00000525991.5:c.*1017C>A	ENSP00000433842.1:n.*1017C>A
ENST00000526814.5:n.1697C>A
ENST00000527420.5:c.*299C>A	ENSP00000433191.1:n.*299C>A
ENST00000527953.5:n.1736C>A
ENST00000533320.5:n.1676C>A
ENST00000535898.5:c.1136C>A	ENSP00000445062.1:p.Pro379His
ENST00000539050.5:c.1232C>A	ENSP00000442343.2:p.Pro411His
ENST00000623108.3:c.1232C>A	ENSP00000485110.1:p.Pro411His
NM_000770.3:c.1442C>A MANE Select	NP_000761.3:p.Pro481His
NM_001198853.1:c.1232C>A	NP_001185782.1:p.Pro411His
NM_001198854.1:c.1136C>A	NP_001185783.1:p.Pro379His
NM_001198855.1:c.1232C>A	NP_001185784.1:p.Pro411His