Canonical Allele Identifier: CA470987373
Gene: CYP2C9 HGNC NCBI

Linked Data

gnomAD v4: 10-94941992-A-C
MyVariant Identifiers: chr10:g.96701749A>C (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94941992A>C , CM000672.2:g.94941992A>C GRCh38
NC_000010.10:g.96701749A>C , CM000672.1:g.96701749A>C GRCh37
NC_000010.9:g.96691739A>C NCBI36
NG_008385.1:g.8335A>C
NG_008385.2:g.8835A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000260682.8:c.303A>C MANE Select ENSP00000260682.6:p.Pro101=
ENST00000643112.1:c.303A>C ENSP00000496202.1:p.Pro101=
ENST00000645207.1:n.456A>C
ENST00000260682.6:c.303A>C ENSP00000260682.6:p.Pro101=
ENST00000461906.1:n.328A>C
ENST00000473496.1:n.74A>C
NM_000771.3:c.303A>C NP_000762.2:p.Pro101=
NM_000771.4:c.303A>C MANE Select NP_000762.2:p.Pro101=
Search 100 bp 5'
Search 100 bp 3'