Canonical Allele Identifier: CA377677643

Gene: CYP2C8

Linked Data

• dbSNP Id: rs756095494
• MyVariant Identifiers: chr10:g.96798666G>C (hg19) ; chr10:g.95038909G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.95038909G>C , CM000672.2:g.95038909G>C	GRCh38
NC_000010.10:g.96798666G>C , CM000672.1:g.96798666G>C	GRCh37
NC_000010.9:g.96788656G>C	NCBI36
NG_007972.1:g.35589C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000371270.6:c.1279C>G MANE Select	ENSP00000360317.3:p.Pro427Ala
ENST00000371270.5:c.1279C>G	ENSP00000360317.3:p.Pro427Ala
ENST00000490994.6:c.*1065C>G	ENSP00000433314.1:n.*1065C>G
ENST00000525991.5:c.*854C>G	ENSP00000433842.1:n.*854C>G
ENST00000526814.5:n.1534C>G
ENST00000527420.5:c.*136C>G	ENSP00000433191.1:n.*136C>G
ENST00000527953.5:n.1573C>G
ENST00000531714.1:n.467C>G
ENST00000533320.5:n.1513C>G
ENST00000535898.5:c.973C>G	ENSP00000445062.1:p.Pro325Ala
ENST00000539050.5:c.1069C>G	ENSP00000442343.2:p.Pro357Ala
ENST00000623108.3:c.1069C>G	ENSP00000485110.1:p.Pro357Ala
NM_000770.3:c.1279C>G MANE Select	NP_000761.3:p.Pro427Ala
NM_001198853.1:c.1069C>G	NP_001185782.1:p.Pro357Ala
NM_001198854.1:c.973C>G	NP_001185783.1:p.Pro325Ala
NM_001198855.1:c.1069C>G	NP_001185784.1:p.Pro357Ala
XR_945610.1:n.1414C>G