Canonical Allele Identifier: CA377676236
Gene: CYP2C9 HGNC NCBI

Linked Data

MyVariant Identifiers: chr10:g.96740996C>G (hg19) chr10:g.94981239C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94981239C>G , CM000672.2:g.94981239C>G GRCh38
NC_000010.10:g.96740996C>G , CM000672.1:g.96740996C>G GRCh37
NC_000010.9:g.96730986C>G NCBI36
NG_008385.1:g.47582C>G
NG_008385.2:g.48082C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000260682.8:c.1018C>G MANE Select ENSP00000260682.6:p.Gln340Glu
ENST00000643112.1:c.*27C>G ENSP00000496202.1:n.*27C>G
ENST00000260682.6:c.1018C>G ENSP00000260682.6:p.Gln340Glu
NM_000771.3:c.1018C>G NP_000762.2:p.Gln340Glu
NM_000771.4:c.1018C>G MANE Select NP_000762.2:p.Gln340Glu
Search 100 bp 5'
Search 100 bp 3'