Canonical Allele Identifier: CA670187978
Gene: CYP2C9 HGNC NCBI

Linked Data

dbSNP Id: rs1433027014
gnomAD v4: 10-94989212-A-C
MyVariant Identifiers: chr10:g.96748969A>C (hg19) chr10:g.94989212A>C (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94989212A>C , CM000672.2:g.94989212A>C GRCh38
NC_000010.10:g.96748969A>C , CM000672.1:g.96748969A>C GRCh37
NC_000010.9:g.96738959A>C NCBI36
NG_008385.1:g.55555A>C
NG_008385.2:g.56055A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000260682.8:c.*184A>C MANE Select ENSP00000260682.6:n.*184A>C
ENST00000643112.1:c.*666A>C ENSP00000496202.1:n.*666A>C
ENST00000260682.6:c.*184A>C ENSP00000260682.6:n.*184A>C
NM_000771.3:c.*184A>C NP_000762.2:n.*184A>C
NM_000771.4:c.*184A>C MANE Select NP_000762.2:n.*184A>C
Search 100 bp 5'
Search 100 bp 3'