Canonical Allele Identifier: CA931385680
Gene: CYP2C9 HGNC NCBI

Linked Data

dbSNP Id: rs2032363902
gnomAD v3: 10-94988823-G-A
gnomAD v4: 10-94988823-G-A
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94988823G>A , CM000672.2:g.94988823G>A GRCh38
NC_000010.10:g.96748580G>A , CM000672.1:g.96748580G>A GRCh37
NC_000010.9:g.96738570G>A NCBI36
NG_008385.1:g.55166G>A
NG_008385.2:g.55666G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000260682.8:c.1292-24G>A MANE Select ENSP00000260682.6:n.1292-24G>A
ENST00000643112.1:c.*301-24G>A ENSP00000496202.1:n.*301-24G>A
ENST00000260682.6:c.1292-24G>A ENSP00000260682.6:n.1292-24G>A
NM_000771.3:c.1292-24G>A NP_000762.2:n.1292-24G>A
NM_000771.4:c.1292-24G>A MANE Select NP_000762.2:n.1292-24G>A
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