Canonical Allele Identifier: CA5617451
Gene: CYP2C8 HGNC NCBI
COSMIC:
COSN163713 (not active)
COSN8863082 (not active)
MyVariant.info:
GRCh38 chr10:g.95037104G>A
GRCh37 chr10:g.96796861G>A
gnomAD v2:
10:96796861 G / A
gnomAD v3:
10:95037104 G / A
gnomAD v4:
chr10-95037104-G-A
Joint Max Group AF 0.40805711 (EAS)
Genomes Max Group AF 0.37766579 (EAS)
Exomes Max Group AF 0.4104847 (EAS)
dbSNP:
1058932
JSON-LD

Genomic Alleles

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

Transcript Alleles

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