Canonical Allele Identifier: CA470832614
Gene: CYP2C9 HGNC NCBI

Linked Data

dbSNP Id: rs1387106559

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94949113C>T , CM000672.2:g.94949113C>T GRCh38
NC_000010.10:g.96708870C>T , CM000672.1:g.96708870C>T GRCh37
NC_000010.9:g.96698860C>T NCBI36
NG_008385.1:g.15456C>T
NG_008385.2:g.15956C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000260682.8:c.648C>T MANE Select ENSP00000260682.6:p.Cys216=
ENST00000643112.1:c.648C>T ENSP00000496202.1:p.Cys216=
ENST00000260682.6:c.648C>T ENSP00000260682.6:p.Cys216=
ENST00000473496.1:n.419C>T
NM_000771.3:c.648C>T NP_000762.2:p.Cys216=
NM_000771.4:c.648C>T MANE Select NP_000762.2:p.Cys216=