Canonical Allele Identifier: CA595334245

Gene: CYP2C8

Linked Data

• dbSNP Id: rs1416576682
• gnomAD v2: 10-96800494-G-A
• gnomAD v3: 10-95040737-G-A
• gnomAD v4: 10-95040737-G-A
• MyVariant Identifiers: chr10:g.96800494G>A (hg19) ; chr10:g.95040737G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.95040737G>A , CM000672.2:g.95040737G>A	GRCh38
NC_000010.10:g.96800494G>A , CM000672.1:g.96800494G>A	GRCh37
NC_000010.9:g.96790484G>A	NCBI36
NG_007972.1:g.33761C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371270.6:c.1150-1699C>T MANE Select	ENSP00000360317.3:n.1150-1699C>T
ENST00000371270.5:c.1150-1699C>T	ENSP00000360317.3:n.1150-1699C>T
ENST00000479946.2:n.1492+185C>T
ENST00000490994.6:c.*936-1699C>T	ENSP00000433314.1:n.*936-1699C>T
ENST00000525991.5:c.*725-1699C>T	ENSP00000433842.1:n.*725-1699C>T
ENST00000526814.5:n.1405-1699C>T
ENST00000527420.5:c.*6+185C>T	ENSP00000433191.1:n.*6+185C>T
ENST00000527953.5:n.1443+185C>T
ENST00000533320.5:n.1384-1699C>T
ENST00000535898.5:c.844-1699C>T	ENSP00000445062.1:n.844-1699C>T
ENST00000539050.5:c.940-1699C>T	ENSP00000442343.2:n.940-1699C>T
ENST00000623108.3:c.940-1699C>T	ENSP00000485110.1:n.940-1699C>T
NM_000770.3:c.1150-1699C>T MANE Select	NP_000761.3:n.1150-1699C>T
NM_001198853.1:c.940-1699C>T	NP_001185782.1:n.940-1699C>T
NM_001198854.1:c.844-1699C>T	NP_001185783.1:n.844-1699C>T
NM_001198855.1:c.940-1699C>T	NP_001185784.1:n.940-1699C>T
XR_945610.1:n.1284+185C>T