Canonical Allele Identifier: CA470837354
Gene: CYP2C9 HGNC NCBI

Linked Data

dbSNP Id: rs1199078693
gnomAD v3: 10-94988860-T-C
gnomAD v4: 10-94988860-T-C
MyVariant Identifiers: chr10:g.96748617T>C (hg19) chr10:g.94988860T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94988860T>C , CM000672.2:g.94988860T>C GRCh38
NC_000010.10:g.96748617T>C , CM000672.1:g.96748617T>C GRCh37
NC_000010.9:g.96738607T>C NCBI36
NG_008385.1:g.55203T>C
NG_008385.2:g.55703T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000260682.8:c.1305T>C MANE Select ENSP00000260682.6:p.Cys435=
ENST00000643112.1:c.*314T>C ENSP00000496202.1:n.*314T>C
ENST00000260682.6:c.1305T>C ENSP00000260682.6:p.Cys435=
NM_000771.3:c.1305T>C NP_000762.2:p.Cys435=
NM_000771.4:c.1305T>C MANE Select NP_000762.2:p.Cys435=
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