Canonical Allele Identifier: CA1929349317
Gene: CYP2C9 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94988755C= , CM000672.2:g.94988755C= GRCh38
NC_000010.10:g.96748512C= , CM000672.1:g.96748512C= GRCh37
NC_000010.9:g.96738502C= NCBI36
NG_008385.1:g.55098C=
NG_008385.2:g.55598C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000260682.8:c.1292-92C= MANE Select ENSP00000260682.6:n.1292-92C=
ENST00000643112.1:c.*301-92C= ENSP00000496202.1:n.*301-92C=
ENST00000260682.6:c.1292-92C= ENSP00000260682.6:n.1292-92C=
NM_000771.3:c.1292-92C= NP_000762.2:n.1292-92C=
NM_000771.4:c.1292-92C= MANE Select NP_000762.2:n.1292-92C=