Canonical Allele Identifier: CA470832085
Gene: CYP2C9 HGNC NCBI

Linked Data

MyVariant Identifiers: chr10:g.96701617C>G (hg19)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94941860C>G , CM000672.2:g.94941860C>G GRCh38
NC_000010.10:g.96701617C>G , CM000672.1:g.96701617C>G GRCh37
NC_000010.9:g.96691607C>G NCBI36
NG_008385.1:g.8203C>G
NG_008385.2:g.8703C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000260682.8:c.171C>G MANE Select ENSP00000260682.6:p.Leu57=
ENST00000643112.1:c.171C>G ENSP00000496202.1:p.Leu57=
ENST00000645207.1:n.324C>G
ENST00000260682.6:c.171C>G ENSP00000260682.6:p.Leu57=
ENST00000461906.1:n.196C>G
NM_000771.3:c.171C>G NP_000762.2:p.Leu57=
NM_000771.4:c.171C>G MANE Select NP_000762.2:p.Leu57=
Search 100 bp 5'
Search 100 bp 3'