Canonical Allele Identifier: CA2610266855
Gene: CYP2C9 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94989092A>G , CM000672.2:g.94989092A>G GRCh38
NC_000010.10:g.96748849A>G , CM000672.1:g.96748849A>G GRCh37
NC_000010.9:g.96738839A>G NCBI36
NG_008385.1:g.55435A>G
NG_008385.2:g.55935A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000260682.8:c.*64A>G MANE Select ENSP00000260682.6:n.*64A>G
ENST00000643112.1:c.*546A>G ENSP00000496202.1:n.*546A>G
ENST00000260682.6:c.*64A>G ENSP00000260682.6:n.*64A>G
NM_000771.3:c.*64A>G NP_000762.2:n.*64A>G
NM_000771.4:c.*64A>G MANE Select NP_000762.2:n.*64A>G