Canonical Allele Identifier: CA377683367

Gene: CYP2C8

Linked Data

• MyVariant Identifiers: chr10:g.96827127G>C (hg19) ; chr10:g.95067370G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.95067370G>C , CM000672.2:g.95067370G>C	GRCh38
NC_000010.10:g.96827127G>C , CM000672.1:g.96827127G>C	GRCh37
NC_000010.9:g.96817117G>C	NCBI36
NG_007972.1:g.7128C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371270.6:c.332-13C>G MANE Select	ENSP00000360317.3:n.332-13C>G
ENST00000371270.5:c.332-13C>G	ENSP00000360317.3:n.332-13C>G
ENST00000479946.2:n.623C>G
ENST00000490994.6:c.*118-13C>G	ENSP00000433314.1:n.*118-13C>G
ENST00000525991.5:c.207-13C>G	ENSP00000433842.1:n.207-13C>G
ENST00000526814.5:n.574C>G
ENST00000527420.5:c.332-13C>G	ENSP00000433191.1:n.332-13C>G
ENST00000527953.5:n.574C>G
ENST00000533320.5:n.553C>G
ENST00000535898.5:c.26-13C>G	ENSP00000445062.1:n.26-13C>G
ENST00000539050.5:c.122-13C>G	ENSP00000442343.2:n.122-13C>G
ENST00000623108.3:c.122-13C>G	ENSP00000485110.1:n.122-13C>G
ENST00000628935.1:c.61C>G	ENSP00000487145.1:p.Leu21Val
NM_000770.3:c.332-13C>G MANE Select	NP_000761.3:n.332-13C>G
NM_001198853.1:c.122-13C>G	NP_001185782.1:n.122-13C>G
NM_001198854.1:c.26-13C>G	NP_001185783.1:n.26-13C>G
NM_001198855.1:c.122-13C>G	NP_001185784.1:n.122-13C>G
XR_945610.1:n.428-13C>G