Canonical Allele Identifier: CA377673951
Gene: CYP2C9 HGNC NCBI

Linked Data

dbSNP Id: rs1327659514
gnomAD v3: 10-94949112-G-A
gnomAD v4: 10-94949112-G-A
MyVariant Identifiers: chr10:g.96708869G>A (hg19) chr10:g.94949112G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94949112G>A , CM000672.2:g.94949112G>A GRCh38
NC_000010.10:g.96708869G>A , CM000672.1:g.96708869G>A GRCh37
NC_000010.9:g.96698859G>A NCBI36
NG_008385.1:g.15455G>A
NG_008385.2:g.15955G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000260682.8:c.647G>A MANE Select ENSP00000260682.6:p.Cys216Tyr
ENST00000643112.1:c.647G>A ENSP00000496202.1:p.Cys216Tyr
ENST00000260682.6:c.647G>A ENSP00000260682.6:p.Cys216Tyr
ENST00000473496.1:n.418G>A
NM_000771.3:c.647G>A NP_000762.2:p.Cys216Tyr
NM_000771.4:c.647G>A MANE Select NP_000762.2:p.Cys216Tyr
Search 100 bp 5'
Search 100 bp 3'