Canonical Allele Identifier: CA377672911
Gene: CYP2C9 HGNC NCBI

Linked Data

gnomAD v4: 10-94942000-A-G
MyVariant Identifiers: chr10:g.96701757A>G (hg19) chr10:g.94942000A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94942000A>G , CM000672.2:g.94942000A>G GRCh38
NC_000010.10:g.96701757A>G , CM000672.1:g.96701757A>G GRCh37
NC_000010.9:g.96691747A>G NCBI36
NG_008385.1:g.8343A>G
NG_008385.2:g.8843A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000260682.8:c.311A>G MANE Select ENSP00000260682.6:p.Glu104Gly
ENST00000643112.1:c.311A>G ENSP00000496202.1:p.Glu104Gly
ENST00000645207.1:n.464A>G
ENST00000260682.6:c.311A>G ENSP00000260682.6:p.Glu104Gly
ENST00000461906.1:n.336A>G
ENST00000473496.1:n.82A>G
NM_000771.3:c.311A>G NP_000762.2:p.Glu104Gly
NM_000771.4:c.311A>G MANE Select NP_000762.2:p.Glu104Gly
Search 100 bp 5'
Search 100 bp 3'