Canonical Allele Identifier: CA377677146
Gene: CYP2C9 HGNC NCBI

Linked Data

dbSNP Id: rs1244582871

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94988996C>A , CM000672.2:g.94988996C>A GRCh38
NC_000010.10:g.96748753C>A , CM000672.1:g.96748753C>A GRCh37
NC_000010.9:g.96738743C>A NCBI36
NG_008385.1:g.55339C>A
NG_008385.2:g.55839C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000260682.8:c.1441C>A MANE Select ENSP00000260682.6:p.Pro481Thr
ENST00000643112.1:c.*450C>A ENSP00000496202.1:n.*450C>A
ENST00000260682.6:c.1441C>A ENSP00000260682.6:p.Pro481Thr
NM_000771.3:c.1441C>A NP_000762.2:p.Pro481Thr
NM_000771.4:c.1441C>A MANE Select NP_000762.2:p.Pro481Thr