Canonical Allele Identifier: CA377672991
Gene: CYP2C9 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94942204G>A , CM000672.2:g.94942204G>A GRCh38
NC_000010.10:g.96701961G>A , CM000672.1:g.96701961G>A GRCh37
NC_000010.9:g.96691951G>A NCBI36
NG_008385.1:g.8547G>A
NG_008385.2:g.9047G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000260682.8:c.344G>A MANE Select ENSP00000260682.6:p.Ser115Asn
ENST00000643112.1:c.344G>A ENSP00000496202.1:p.Ser115Asn
ENST00000645207.1:n.497G>A
ENST00000260682.6:c.344G>A ENSP00000260682.6:p.Ser115Asn
ENST00000461906.1:n.369G>A
ENST00000473496.1:n.115G>A
NM_000771.3:c.344G>A NP_000762.2:p.Ser115Asn
NM_000771.4:c.344G>A MANE Select NP_000762.2:p.Ser115Asn