Canonical Allele Identifier: CA211714284

Gene: CYP2C8

Linked Data

• dbSNP Id: rs555931580
• gnomAD v4: 10-95040945-T-C
• MyVariant Identifiers: chr10:g.96800702T>C (hg19) ; chr10:g.95040945T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.95040945T>C , CM000672.2:g.95040945T>C	GRCh38
NC_000010.10:g.96800702T>C , CM000672.1:g.96800702T>C	GRCh37
NC_000010.9:g.96790692T>C	NCBI36
NG_007972.1:g.33553A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371270.6:c.1150-1907A>G MANE Select	ENSP00000360317.3:n.1150-1907A>G
ENST00000371270.5:c.1150-1907A>G	ENSP00000360317.3:n.1150-1907A>G
ENST00000479946.2:n.1469A>G
ENST00000490994.6:c.*936-1907A>G	ENSP00000433314.1:n.*936-1907A>G
ENST00000525991.5:c.*725-1907A>G	ENSP00000433842.1:n.*725-1907A>G
ENST00000526814.5:n.1405-1907A>G
ENST00000527420.5:c.1165A>G	ENSP00000433191.1:p.Ile389Val
ENST00000527953.5:n.1420A>G
ENST00000533320.5:n.1384-1907A>G
ENST00000535898.5:c.844-1907A>G	ENSP00000445062.1:n.844-1907A>G
ENST00000539050.5:c.940-1907A>G	ENSP00000442343.2:n.940-1907A>G
ENST00000623108.3:c.940-1907A>G	ENSP00000485110.1:n.940-1907A>G
ENST00000628935.1:c.907A>G	ENSP00000487145.1:p.Ile303Val
NM_000770.3:c.1150-1907A>G MANE Select	NP_000761.3:n.1150-1907A>G
NM_001198853.1:c.940-1907A>G	NP_001185782.1:n.940-1907A>G
NM_001198854.1:c.844-1907A>G	NP_001185783.1:n.844-1907A>G
NM_001198855.1:c.940-1907A>G	NP_001185784.1:n.940-1907A>G
XR_945610.1:n.1261A>G