Canonical Allele Identifier: CA377677108
Gene: CYP2C9 HGNC NCBI

Linked Data

dbSNP Id: rs2032367182
MyVariant Identifiers: chr10:g.96748732A>C (hg19) chr10:g.94988975A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94988975A>C , CM000672.2:g.94988975A>C GRCh38
NC_000010.10:g.96748732A>C , CM000672.1:g.96748732A>C GRCh37
NC_000010.9:g.96738722A>C NCBI36
NG_008385.1:g.55318A>C
NG_008385.2:g.55818A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000260682.8:c.1420A>C MANE Select ENSP00000260682.6:p.Asn474His
ENST00000643112.1:c.*429A>C ENSP00000496202.1:n.*429A>C
ENST00000260682.6:c.1420A>C ENSP00000260682.6:p.Asn474His
NM_000771.3:c.1420A>C NP_000762.2:p.Asn474His
NM_000771.4:c.1420A>C MANE Select NP_000762.2:p.Asn474His
Search 100 bp 5'
Search 100 bp 3'