Canonical Allele Identifier: CA1929375058

Gene: CYP2C8

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.95037104G>C , CM000672.2:g.95037104G>C	GRCh38
NC_000010.10:g.96796861G>C , CM000672.1:g.96796861G>C	GRCh37
NC_000010.9:g.96786851G>C	NCBI36
NG_007972.1:g.37394C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371270.6:c.*24C>G MANE Select	ENSP00000360317.3:n.*24C>G
ENST00000371270.5:c.*24C>G	ENSP00000360317.3:n.*24C>G
ENST00000490994.6:c.*1283C>G	ENSP00000433314.1:n.*1283C>G
ENST00000525991.5:c.*1072C>G	ENSP00000433842.1:n.*1072C>G
ENST00000526814.5:n.1752C>G
ENST00000527420.5:c.*354C>G	ENSP00000433191.1:n.*354C>G
ENST00000527953.5:n.1791C>G
ENST00000533320.5:n.1731C>G
ENST00000535898.5:c.*24C>G	ENSP00000445062.1:n.*24C>G
ENST00000539050.5:c.*24C>G	ENSP00000442343.2:n.*24C>G
ENST00000623108.3:c.*24C>G	ENSP00000485110.1:n.*24C>G
NM_000770.3:c.*24C>G MANE Select	NP_000761.3:n.*24C>G
NM_001198853.1:c.*24C>G	NP_001185782.1:n.*24C>G
NM_001198854.1:c.*24C>G	NP_001185783.1:n.*24C>G
NM_001198855.1:c.*24C>G	NP_001185784.1:n.*24C>G