Canonical Allele Identifier: CA1929349561
Gene: CYP2C9 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94988879G= , CM000672.2:g.94988879G= GRCh38
NC_000010.10:g.96748636G= , CM000672.1:g.96748636G= GRCh37
NC_000010.9:g.96738626G= NCBI36
NG_008385.1:g.55222G=
NG_008385.2:g.55722G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000260682.8:c.1324G= MANE Select ENSP00000260682.6:p.Gly442=
ENST00000643112.1:c.*333G= ENSP00000496202.1:n.*333G=
ENST00000260682.6:c.1324G= ENSP00000260682.6:p.Gly442=
NM_000771.3:c.1324G= NP_000762.2:p.Gly442=
NM_000771.4:c.1324G= MANE Select NP_000762.2:p.Gly442=
Search 100 bp 5'
Search 100 bp 3'