Canonical Allele Identifier: CA211711862

Gene: CYP2C8

Linked Data

• dbSNP Id: rs920502935
• gnomAD v3: 10-95037711-G-A
• gnomAD v4: 10-95037711-G-A
• MyVariant Identifiers: chr10:g.96797468G>A (hg19) ; chr10:g.95037711G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.95037711G>A , CM000672.2:g.95037711G>A	GRCh38
NC_000010.10:g.96797468G>A , CM000672.1:g.96797468G>A	GRCh37
NC_000010.9:g.96787458G>A	NCBI36
NG_007972.1:g.36787C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371270.6:c.1292-402C>T MANE Select	ENSP00000360317.3:n.1292-402C>T
ENST00000371270.5:c.1292-402C>T	ENSP00000360317.3:n.1292-402C>T
ENST00000490994.6:c.*1078-402C>T	ENSP00000433314.1:n.*1078-402C>T
ENST00000525991.5:c.*867-402C>T	ENSP00000433842.1:n.*867-402C>T
ENST00000526814.5:n.1547-402C>T
ENST00000527420.5:c.*149-402C>T	ENSP00000433191.1:n.*149-402C>T
ENST00000527953.5:n.1586-402C>T
ENST00000531714.1:n.480-402C>T
ENST00000533320.5:n.1526-402C>T
ENST00000535898.5:c.986-402C>T	ENSP00000445062.1:n.986-402C>T
ENST00000539050.5:c.1082-402C>T	ENSP00000442343.2:n.1082-402C>T
ENST00000623108.3:c.1082-402C>T	ENSP00000485110.1:n.1082-402C>T
NM_000770.3:c.1292-402C>T MANE Select	NP_000761.3:n.1292-402C>T
NM_001198853.1:c.1082-402C>T	NP_001185782.1:n.1082-402C>T
NM_001198854.1:c.986-402C>T	NP_001185783.1:n.986-402C>T
NM_001198855.1:c.1082-402C>T	NP_001185784.1:n.1082-402C>T
XR_945610.1:n.1427-402C>T