Canonical Allele Identifier: CA1929292093
Gene: CYP2C9 HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94941721T= , CM000672.2:g.94941721T= GRCh38
NC_000010.10:g.96701478T= , CM000672.1:g.96701478T= GRCh37
NC_000010.9:g.96691468T= NCBI36
NG_008385.1:g.8064T=
NG_008385.2:g.8564T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000260682.8:c.169-137T= MANE Select ENSP00000260682.6:n.169-137T=
ENST00000643112.1:c.169-137T= ENSP00000496202.1:n.169-137T=
ENST00000645207.1:n.185T=
ENST00000260682.6:c.169-137T= ENSP00000260682.6:n.169-137T=
ENST00000461906.1:n.194-137T=
NM_000771.3:c.169-137T= NP_000762.2:n.169-137T=
NM_000771.4:c.169-137T= MANE Select NP_000762.2:n.169-137T=
Search 100 bp 5'
Search 100 bp 3'