Canonical Allele Identifier: CA1929298173
Gene: CYP2C9 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94949036C= , CM000672.2:g.94949036C= GRCh38
NC_000010.10:g.96708793C= , CM000672.1:g.96708793C= GRCh37
NC_000010.9:g.96698783C= NCBI36
NG_008385.1:g.15379C=
NG_008385.2:g.15879C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000260682.8:c.643-72C= MANE Select ENSP00000260682.6:n.643-72C=
ENST00000643112.1:c.643-72C= ENSP00000496202.1:n.643-72C=
ENST00000260682.6:c.643-72C= ENSP00000260682.6:n.643-72C=
ENST00000473496.1:n.414-72C=
NM_000771.3:c.643-72C= NP_000762.2:n.643-72C=
NM_000771.4:c.643-72C= MANE Select NP_000762.2:n.643-72C=
Search 100 bp 5'
Search 100 bp 3'