Canonical Allele Identifier: CA1929292250
Gene: CYP2C9 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94941993C= , CM000672.2:g.94941993C= GRCh38
NC_000010.10:g.96701750C= , CM000672.1:g.96701750C= GRCh37
NC_000010.9:g.96691740C= NCBI36
NG_008385.1:g.8336C=
NG_008385.2:g.8836C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000260682.8:c.304C= MANE Select ENSP00000260682.6:p.Leu102=
ENST00000643112.1:c.304C= ENSP00000496202.1:p.Leu102=
ENST00000645207.1:n.457C=
ENST00000260682.6:c.304C= ENSP00000260682.6:p.Leu102=
ENST00000461906.1:n.329C=
ENST00000473496.1:n.75C=
NM_000771.3:c.304C= NP_000762.2:p.Leu102=
NM_000771.4:c.304C= MANE Select NP_000762.2:p.Leu102=