Canonical Allele Identifier: CA1929349351
Gene: CYP2C9 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94988786T= , CM000672.2:g.94988786T= GRCh38
NC_000010.10:g.96748543T= , CM000672.1:g.96748543T= GRCh37
NC_000010.9:g.96738533T= NCBI36
NG_008385.1:g.55129T=
NG_008385.2:g.55629T=

Transcript Alleles

HGVS Amino-acid change
ENST00000260682.8:c.1292-61T= MANE Select ENSP00000260682.6:n.1292-61T=
ENST00000643112.1:c.*301-61T= ENSP00000496202.1:n.*301-61T=
ENST00000260682.6:c.1292-61T= ENSP00000260682.6:n.1292-61T=
NM_000771.3:c.1292-61T= NP_000762.2:n.1292-61T=
NM_000771.4:c.1292-61T= MANE Select NP_000762.2:n.1292-61T=
Search 100 bp 5'
Search 100 bp 3'