Canonical Allele Identifier: CA377676182
Gene: CYP2C9 HGNC NCBI

Linked Data

MyVariant Identifiers: chr10:g.96740970T>G (hg19) chr10:g.94981213T>G (hg38)
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Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid change
ENST00000260682.8:c.992T>G MANE Select ENSP00000260682.6:p.Ile331Ser
ENST00000643112.1:c.*1T>G ENSP00000496202.1:n.*1T>G
ENST00000260682.6:c.992T>G ENSP00000260682.6:p.Ile331Ser
NM_000771.3:c.992T>G NP_000762.2:p.Ile331Ser
NM_000771.4:c.992T>G MANE Select NP_000762.2:p.Ile331Ser
Search 100 bp 5'
Search 100 bp 3'