Canonical Allele Identifier: CA1929349877
Gene: CYP2C9 HGNC NCBI

Linked Data

dbSNP Id: rs2032370084
gnomAD v4: 10-94989098-C-A
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94989098C>A , CM000672.2:g.94989098C>A GRCh38
NC_000010.10:g.96748855C>A , CM000672.1:g.96748855C>A GRCh37
NC_000010.9:g.96738845C>A NCBI36
NG_008385.1:g.55441C>A
NG_008385.2:g.55941C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000260682.8:c.*70C>A MANE Select ENSP00000260682.6:n.*70C>A
ENST00000643112.1:c.*552C>A ENSP00000496202.1:n.*552C>A
ENST00000260682.6:c.*70C>A ENSP00000260682.6:n.*70C>A
NM_000771.3:c.*70C>A NP_000762.2:n.*70C>A
NM_000771.4:c.*70C>A MANE Select NP_000762.2:n.*70C>A
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