Canonical Allele Identifier: CA377677624

Gene: CYP2C8

Linked Data

• dbSNP Id: rs2134405724
• MyVariant Identifiers: chr10:g.96798657C>A (hg19) ; chr10:g.95038900C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.95038900C>A , CM000672.2:g.95038900C>A	GRCh38
NC_000010.10:g.96798657C>A , CM000672.1:g.96798657C>A	GRCh37
NC_000010.9:g.96788647C>A	NCBI36
NG_007972.1:g.35598G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000371270.6:c.1288G>T MANE Select	ENSP00000360317.3:p.Ala430Ser
ENST00000371270.5:c.1288G>T	ENSP00000360317.3:p.Ala430Ser
ENST00000490994.6:c.*1074G>T	ENSP00000433314.1:n.*1074G>T
ENST00000525991.5:c.*863G>T	ENSP00000433842.1:n.*863G>T
ENST00000526814.5:n.1543G>T
ENST00000527420.5:c.*145G>T	ENSP00000433191.1:n.*145G>T
ENST00000527953.5:n.1582G>T
ENST00000531714.1:n.476G>T
ENST00000533320.5:n.1522G>T
ENST00000535898.5:c.982G>T	ENSP00000445062.1:p.Ala328Ser
ENST00000539050.5:c.1078G>T	ENSP00000442343.2:p.Ala360Ser
ENST00000623108.3:c.1078G>T	ENSP00000485110.1:p.Ala360Ser
NM_000770.3:c.1288G>T MANE Select	NP_000761.3:p.Ala430Ser
NM_001198853.1:c.1078G>T	NP_001185782.1:p.Ala360Ser
NM_001198854.1:c.982G>T	NP_001185783.1:p.Ala328Ser
NM_001198855.1:c.1078G>T	NP_001185784.1:p.Ala360Ser
XR_945610.1:n.1423G>T