Canonical Allele Identifier: CA377672895
Gene: CYP2C9 HGNC NCBI

Linked Data

MyVariant Identifiers: chr10:g.96701748C>G (hg19) chr10:g.94941991C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94941991C>G , CM000672.2:g.94941991C>G GRCh38
NC_000010.10:g.96701748C>G , CM000672.1:g.96701748C>G GRCh37
NC_000010.9:g.96691738C>G NCBI36
NG_008385.1:g.8334C>G
NG_008385.2:g.8834C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000260682.8:c.302C>G MANE Select ENSP00000260682.6:p.Pro101Arg
ENST00000643112.1:c.302C>G ENSP00000496202.1:p.Pro101Arg
ENST00000645207.1:n.455C>G
ENST00000260682.6:c.302C>G ENSP00000260682.6:p.Pro101Arg
ENST00000461906.1:n.327C>G
ENST00000473496.1:n.73C>G
NM_000771.3:c.302C>G NP_000762.2:p.Pro101Arg
NM_000771.4:c.302C>G MANE Select NP_000762.2:p.Pro101Arg
Search 100 bp 5'
Search 100 bp 3'