Canonical Allele Identifier: CA931384610
Gene: CYP2C9 HGNC NCBI

Linked Data

dbSNP Id: rs2031517836
gnomAD v3: 10-94947534-A-G
gnomAD v4: 10-94947534-A-G
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94947534A>G , CM000672.2:g.94947534A>G GRCh38
NC_000010.10:g.96707291A>G , CM000672.1:g.96707291A>G GRCh37
NC_000010.9:g.96697281A>G NCBI36
NG_008385.1:g.13877A>G
NG_008385.2:g.14377A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000260682.8:c.482-245A>G MANE Select ENSP00000260682.6:n.482-245A>G
ENST00000643112.1:c.482-245A>G ENSP00000496202.1:n.482-245A>G
ENST00000645207.1:n.635-245A>G
ENST00000260682.6:c.482-245A>G ENSP00000260682.6:n.482-245A>G
ENST00000473496.1:n.253-245A>G
NM_000771.3:c.482-245A>G NP_000762.2:n.482-245A>G
NM_000771.4:c.482-245A>G MANE Select NP_000762.2:n.482-245A>G
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