Canonical Allele Identifier: CA1929341769
Gene: CYP2C9 HGNC NCBI

Linked Data

dbSNP Id: rs1159605181
gnomAD v4: 10-94981131-C-A
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94981131C>A , CM000672.2:g.94981131C>A GRCh38
NC_000010.10:g.96740888C>A , CM000672.1:g.96740888C>A GRCh37
NC_000010.9:g.96730878C>A NCBI36
NG_008385.1:g.47474C>A
NG_008385.2:g.47974C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000260682.8:c.962-52C>A MANE Select ENSP00000260682.6:n.962-52C>A
ENST00000643112.1:c.820-52C>A ENSP00000496202.1:n.820-52C>A
ENST00000260682.6:c.962-52C>A ENSP00000260682.6:n.962-52C>A
NM_000771.3:c.962-52C>A NP_000762.2:n.962-52C>A
NM_000771.4:c.962-52C>A MANE Select NP_000762.2:n.962-52C>A
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