Canonical Allele Identifier: CA377683413

Gene: CYP2C8

Linked Data

• dbSNP Id: rs1344289142
• gnomAD v3: 10-95067382-G-A
• gnomAD v4: 10-95067382-G-A
• MyVariant Identifiers: chr10:g.96827139G>A (hg19) ; chr10:g.95067382G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.95067382G>A , CM000672.2:g.95067382G>A	GRCh38
NC_000010.10:g.96827139G>A , CM000672.1:g.96827139G>A	GRCh37
NC_000010.9:g.96817129G>A	NCBI36
NG_007972.1:g.7116C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371270.6:c.332-25C>T MANE Select	ENSP00000360317.3:n.332-25C>T
ENST00000371270.5:c.332-25C>T	ENSP00000360317.3:n.332-25C>T
ENST00000479946.2:n.611C>T
ENST00000490994.6:c.*118-25C>T	ENSP00000433314.1:n.*118-25C>T
ENST00000525991.5:c.207-25C>T	ENSP00000433842.1:n.207-25C>T
ENST00000526814.5:n.562C>T
ENST00000527420.5:c.332-25C>T	ENSP00000433191.1:n.332-25C>T
ENST00000527953.5:n.562C>T
ENST00000533320.5:n.541C>T
ENST00000535898.5:c.26-25C>T	ENSP00000445062.1:n.26-25C>T
ENST00000539050.5:c.122-25C>T	ENSP00000442343.2:n.122-25C>T
ENST00000623108.3:c.122-25C>T	ENSP00000485110.1:n.122-25C>T
ENST00000628935.1:c.49C>T	ENSP00000487145.1:p.Gln17Ter
NM_000770.3:c.332-25C>T MANE Select	NP_000761.3:n.332-25C>T
NM_001198853.1:c.122-25C>T	NP_001185782.1:n.122-25C>T
NM_001198854.1:c.26-25C>T	NP_001185783.1:n.26-25C>T
NM_001198855.1:c.122-25C>T	NP_001185784.1:n.122-25C>T
XR_945610.1:n.428-25C>T