Canonical Allele Identifier: CA5617403
Gene: CYP2C9 HGNC NCBI

Linked Data

dbSNP Id: rs202201137

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94988925A>G , CM000672.2:g.94988925A>G GRCh38
NC_000010.10:g.96748682A>G , CM000672.1:g.96748682A>G GRCh37
NC_000010.9:g.96738672A>G NCBI36
NG_008385.1:g.55268A>G
NG_008385.2:g.55768A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000260682.8:c.1370A>G MANE Select ENSP00000260682.6:p.Asn457Ser
ENST00000643112.1:c.*379A>G ENSP00000496202.1:n.*379A>G
ENST00000260682.6:c.1370A>G ENSP00000260682.6:p.Asn457Ser
NM_000771.3:c.1370A>G NP_000762.2:p.Asn457Ser
NM_000771.4:c.1370A>G MANE Select NP_000762.2:p.Asn457Ser