Canonical Allele Identifier: CA670187378
Gene: CYP2C9 HGNC NCBI

Linked Data

dbSNP Id: rs1435185191

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94988782A>G , CM000672.2:g.94988782A>G GRCh38
NC_000010.10:g.96748539A>G , CM000672.1:g.96748539A>G GRCh37
NC_000010.9:g.96738529A>G NCBI36
NG_008385.1:g.55125A>G
NG_008385.2:g.55625A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000260682.8:c.1292-65A>G MANE Select ENSP00000260682.6:n.1292-65A>G
ENST00000643112.1:c.*301-65A>G ENSP00000496202.1:n.*301-65A>G
ENST00000260682.6:c.1292-65A>G ENSP00000260682.6:n.1292-65A>G
NM_000771.3:c.1292-65A>G NP_000762.2:n.1292-65A>G
NM_000771.4:c.1292-65A>G MANE Select NP_000762.2:n.1292-65A>G