Canonical Allele Identifier: CA1929334729
Gene: CYP2C9 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94974441T= , CM000672.2:g.94974441T= GRCh38
NC_000010.10:g.96734198T= , CM000672.1:g.96734198T= GRCh37
NC_000010.9:g.96724188T= NCBI36
NG_008385.1:g.40784T=
NG_008385.2:g.41284T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000260682.8:c.961+2196T= MANE Select ENSP00000260682.6:n.961+2196T=
ENST00000643112.1:c.820-6742T= ENSP00000496202.1:n.820-6742T=
ENST00000260682.6:c.961+2196T= ENSP00000260682.6:n.961+2196T=
NM_000771.3:c.961+2196T= NP_000762.2:n.961+2196T=
NM_000771.4:c.961+2196T= MANE Select NP_000762.2:n.961+2196T=
Search 100 bp 5'
Search 100 bp 3'