Canonical Allele Identifier: CA470837362
Gene: CYP2C9 HGNC NCBI

Linked Data

dbSNP Id: rs1389026373
gnomAD v2: 10-96748629-C-T
gnomAD v4: 10-94988872-C-T
MyVariant Identifiers: chr10:g.96748629C>T (hg19) chr10:g.94988872C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94988872C>T , CM000672.2:g.94988872C>T GRCh38
NC_000010.10:g.96748629C>T , CM000672.1:g.96748629C>T GRCh37
NC_000010.9:g.96738619C>T NCBI36
NG_008385.1:g.55215C>T
NG_008385.2:g.55715C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000260682.8:c.1317C>T MANE Select ENSP00000260682.6:p.Ala439=
ENST00000643112.1:c.*326C>T ENSP00000496202.1:n.*326C>T
ENST00000260682.6:c.1317C>T ENSP00000260682.6:p.Ala439=
NM_000771.3:c.1317C>T NP_000762.2:p.Ala439=
NM_000771.4:c.1317C>T MANE Select NP_000762.2:p.Ala439=
Search 100 bp 5'
Search 100 bp 3'