Canonical Allele Identifier: CA1929341866
Gene: CYP2C9 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94981171G= , CM000672.2:g.94981171G= GRCh38
NC_000010.10:g.96740928G= , CM000672.1:g.96740928G= GRCh37
NC_000010.9:g.96730918G= NCBI36
NG_008385.1:g.47514G=
NG_008385.2:g.48014G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000260682.8:c.962-12G= MANE Select ENSP00000260682.6:n.962-12G=
ENST00000643112.1:c.820-12G= ENSP00000496202.1:n.820-12G=
ENST00000260682.6:c.962-12G= ENSP00000260682.6:n.962-12G=
NM_000771.3:c.962-12G= NP_000762.2:n.962-12G=
NM_000771.4:c.962-12G= MANE Select NP_000762.2:n.962-12G=
Search 100 bp 5'
Search 100 bp 3'