Canonical Allele Identifier: CA2574622609
Gene: CYP2C9 HGNC NCBI

Linked Data

gnomAD v4: 10-94989055-T-A
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94989055T>A , CM000672.2:g.94989055T>A GRCh38
NC_000010.10:g.96748812T>A , CM000672.1:g.96748812T>A GRCh37
NC_000010.9:g.96738802T>A NCBI36
NG_008385.1:g.55398T>A
NG_008385.2:g.55898T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000260682.8:c.*27T>A MANE Select ENSP00000260682.6:n.*27T>A
ENST00000643112.1:c.*509T>A ENSP00000496202.1:n.*509T>A
ENST00000260682.6:c.*27T>A ENSP00000260682.6:n.*27T>A
NM_000771.3:c.*27T>A NP_000762.2:n.*27T>A
NM_000771.4:c.*27T>A MANE Select NP_000762.2:n.*27T>A
Search 100 bp 5'
Search 100 bp 3'