Canonical Allele Identifier: CA377677612

Gene: CYP2C8

Linked Data

• MyVariant Identifiers: chr10:g.96798652A>C (hg19) ; chr10:g.95038895A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.95038895A>C , CM000672.2:g.95038895A>C	GRCh38
NC_000010.10:g.96798652A>C , CM000672.1:g.96798652A>C	GRCh37
NC_000010.9:g.96788642A>C	NCBI36
NG_007972.1:g.35603T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000371270.6:c.1291+2T>G MANE Select	ENSP00000360317.3:n.1291+2T>G
ENST00000371270.5:c.1291+2T>G	ENSP00000360317.3:n.1291+2T>G
ENST00000490994.6:c.*1077+2T>G	ENSP00000433314.1:n.*1077+2T>G
ENST00000525991.5:c.*866+2T>G	ENSP00000433842.1:n.*866+2T>G
ENST00000526814.5:n.1546+2T>G
ENST00000527420.5:c.*148+2T>G	ENSP00000433191.1:n.*148+2T>G
ENST00000527953.5:n.1585+2T>G
ENST00000531714.1:n.479+2T>G
ENST00000533320.5:n.1525+2T>G
ENST00000535898.5:c.985+2T>G	ENSP00000445062.1:n.985+2T>G
ENST00000539050.5:c.1081+2T>G	ENSP00000442343.2:n.1081+2T>G
ENST00000623108.3:c.1081+2T>G	ENSP00000485110.1:n.1081+2T>G
NM_000770.3:c.1291+2T>G MANE Select	NP_000761.3:n.1291+2T>G
NM_001198853.1:c.1081+2T>G	NP_001185782.1:n.1081+2T>G
NM_001198854.1:c.985+2T>G	NP_001185783.1:n.985+2T>G
NM_001198855.1:c.1081+2T>G	NP_001185784.1:n.1081+2T>G
XR_945610.1:n.1426+2T>G