Canonical Allele Identifier: CA2789073516
Gene: CYP2C9 HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94974514C>A , CM000672.2:g.94974514C>A GRCh38
NC_000010.10:g.96734271C>A , CM000672.1:g.96734271C>A GRCh37
NC_000010.9:g.96724261C>A NCBI36
NG_008385.1:g.40857C>A
NG_008385.2:g.41357C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000260682.8:c.961+2269C>A MANE Select ENSP00000260682.6:n.961+2269C>A
ENST00000643112.1:c.820-6669C>A ENSP00000496202.1:n.820-6669C>A
ENST00000260682.6:c.961+2269C>A ENSP00000260682.6:n.961+2269C>A
NM_000771.3:c.961+2269C>A NP_000762.2:n.961+2269C>A
NM_000771.4:c.961+2269C>A MANE Select NP_000762.2:n.961+2269C>A
Search 100 bp 5'
Search 100 bp 3'