Canonical Allele Identifier: CA377677961

Gene: CYP2C8

Linked Data

• MyVariant Identifiers: chr10:g.96800701A>C (hg19) ; chr10:g.95040944A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.95040944A>C , CM000672.2:g.95040944A>C	GRCh38
NC_000010.10:g.96800701A>C , CM000672.1:g.96800701A>C	GRCh37
NC_000010.9:g.96790691A>C	NCBI36
NG_007972.1:g.33554T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000371270.6:c.1150-1906T>G MANE Select	ENSP00000360317.3:n.1150-1906T>G
ENST00000371270.5:c.1150-1906T>G	ENSP00000360317.3:n.1150-1906T>G
ENST00000479946.2:n.1470T>G
ENST00000490994.6:c.*936-1906T>G	ENSP00000433314.1:n.*936-1906T>G
ENST00000525991.5:c.*725-1906T>G	ENSP00000433842.1:n.*725-1906T>G
ENST00000526814.5:n.1405-1906T>G
ENST00000527420.5:c.1166T>G	ENSP00000433191.1:p.Ile389Arg
ENST00000527953.5:n.1421T>G
ENST00000533320.5:n.1384-1906T>G
ENST00000535898.5:c.844-1906T>G	ENSP00000445062.1:n.844-1906T>G
ENST00000539050.5:c.940-1906T>G	ENSP00000442343.2:n.940-1906T>G
ENST00000623108.3:c.940-1906T>G	ENSP00000485110.1:n.940-1906T>G
ENST00000628935.1:c.908T>G	ENSP00000487145.1:p.Ile303Arg
NM_000770.3:c.1150-1906T>G MANE Select	NP_000761.3:n.1150-1906T>G
NM_001198853.1:c.940-1906T>G	NP_001185782.1:n.940-1906T>G
NM_001198854.1:c.844-1906T>G	NP_001185783.1:n.844-1906T>G
NM_001198855.1:c.940-1906T>G	NP_001185784.1:n.940-1906T>G
XR_945610.1:n.1262T>G