Canonical Allele Identifier: CA1929298161
Gene: CYP2C9 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94949029T= , CM000672.2:g.94949029T= GRCh38
NC_000010.10:g.96708786T= , CM000672.1:g.96708786T= GRCh37
NC_000010.9:g.96698776T= NCBI36
NG_008385.1:g.15372T=
NG_008385.2:g.15872T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000260682.8:c.643-79T= MANE Select ENSP00000260682.6:n.643-79T=
ENST00000643112.1:c.643-79T= ENSP00000496202.1:n.643-79T=
ENST00000260682.6:c.643-79T= ENSP00000260682.6:n.643-79T=
ENST00000473496.1:n.414-79T=
NM_000771.3:c.643-79T= NP_000762.2:n.643-79T=
NM_000771.4:c.643-79T= MANE Select NP_000762.2:n.643-79T=
Search 100 bp 5'
Search 100 bp 3'