Canonical Allele Identifier: CA377673034
Gene: CYP2C9 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94942221A>G , CM000672.2:g.94942221A>G GRCh38
NC_000010.10:g.96701978A>G , CM000672.1:g.96701978A>G GRCh37
NC_000010.9:g.96691968A>G NCBI36
NG_008385.1:g.8564A>G
NG_008385.2:g.9064A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000260682.8:c.361A>G MANE Select ENSP00000260682.6:p.Lys121Glu
ENST00000643112.1:c.361A>G ENSP00000496202.1:p.Lys121Glu
ENST00000645207.1:n.514A>G
ENST00000260682.6:c.361A>G ENSP00000260682.6:p.Lys121Glu
ENST00000461906.1:n.386A>G
ENST00000473496.1:n.132A>G
NM_000771.3:c.361A>G NP_000762.2:p.Lys121Glu
NM_000771.4:c.361A>G MANE Select NP_000762.2:p.Lys121Glu