Canonical Allele Identifier: CA377676181
Gene: CYP2C9 HGNC NCBI

Linked Data

dbSNP Id: rs1433742100
gnomAD v4: 10-94981213-T-C
MyVariant Identifiers: chr10:g.96740970T>C (hg19) chr10:g.94981213T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94981213T>C , CM000672.2:g.94981213T>C GRCh38
NC_000010.10:g.96740970T>C , CM000672.1:g.96740970T>C GRCh37
NC_000010.9:g.96730960T>C NCBI36
NG_008385.1:g.47556T>C
NG_008385.2:g.48056T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000260682.8:c.992T>C MANE Select ENSP00000260682.6:p.Ile331Thr
ENST00000643112.1:c.*1T>C ENSP00000496202.1:n.*1T>C
ENST00000260682.6:c.992T>C ENSP00000260682.6:p.Ile331Thr
NM_000771.3:c.992T>C NP_000762.2:p.Ile331Thr
NM_000771.4:c.992T>C MANE Select NP_000762.2:p.Ile331Thr
Search 100 bp 5'
Search 100 bp 3'