Canonical Allele Identifier: CA931390403

Gene: CYP2C8

Linked Data

• dbSNP Id: rs2032976392
• gnomAD v3: 10-95040687-C-A
• gnomAD v4: 10-95040687-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.95040687C>A , CM000672.2:g.95040687C>A	GRCh38
NC_000010.10:g.96800444C>A , CM000672.1:g.96800444C>A	GRCh37
NC_000010.9:g.96790434C>A	NCBI36
NG_007972.1:g.33811G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371270.6:c.1150-1649G>T MANE Select	ENSP00000360317.3:n.1150-1649G>T
ENST00000371270.5:c.1150-1649G>T	ENSP00000360317.3:n.1150-1649G>T
ENST00000479946.2:n.1492+235G>T
ENST00000490994.6:c.*936-1649G>T	ENSP00000433314.1:n.*936-1649G>T
ENST00000525991.5:c.*725-1649G>T	ENSP00000433842.1:n.*725-1649G>T
ENST00000526814.5:n.1405-1649G>T
ENST00000527420.5:c.*6+235G>T	ENSP00000433191.1:n.*6+235G>T
ENST00000527953.5:n.1443+235G>T
ENST00000533320.5:n.1384-1649G>T
ENST00000535898.5:c.844-1649G>T	ENSP00000445062.1:n.844-1649G>T
ENST00000539050.5:c.940-1649G>T	ENSP00000442343.2:n.940-1649G>T
ENST00000623108.3:c.940-1649G>T	ENSP00000485110.1:n.940-1649G>T
NM_000770.3:c.1150-1649G>T MANE Select	NP_000761.3:n.1150-1649G>T
NM_001198853.1:c.940-1649G>T	NP_001185782.1:n.940-1649G>T
NM_001198854.1:c.844-1649G>T	NP_001185783.1:n.844-1649G>T
NM_001198855.1:c.940-1649G>T	NP_001185784.1:n.940-1649G>T
XR_945610.1:n.1284+235G>T