Canonical Allele Identifier: CA670178388
Gene: CYP2C9 HGNC NCBI

Linked Data

dbSNP Id: rs1321680290
gnomAD v3: 10-94974513-C-A
gnomAD v4: 10-94974513-C-A
MyVariant Identifiers: chr10:g.96734270C>A (hg19) chr10:g.94974513C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94974513C>A , CM000672.2:g.94974513C>A GRCh38
NC_000010.10:g.96734270C>A , CM000672.1:g.96734270C>A GRCh37
NC_000010.9:g.96724260C>A NCBI36
NG_008385.1:g.40856C>A
NG_008385.2:g.41356C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000260682.8:c.961+2268C>A MANE Select ENSP00000260682.6:n.961+2268C>A
ENST00000643112.1:c.820-6670C>A ENSP00000496202.1:n.820-6670C>A
ENST00000260682.6:c.961+2268C>A ENSP00000260682.6:n.961+2268C>A
NM_000771.3:c.961+2268C>A NP_000762.2:n.961+2268C>A
NM_000771.4:c.961+2268C>A MANE Select NP_000762.2:n.961+2268C>A
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