Canonical Allele Identifier: CA595638884
Gene: CYP2C9 HGNC NCBI

Linked Data

dbSNP Id: rs775537358

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94989052T>A , CM000672.2:g.94989052T>A GRCh38
NC_000010.10:g.96748809T>A , CM000672.1:g.96748809T>A GRCh37
NC_000010.9:g.96738799T>A NCBI36
NG_008385.1:g.55395T>A
NG_008385.2:g.55895T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000260682.8:c.*24T>A MANE Select ENSP00000260682.6:n.*24T>A
ENST00000643112.1:c.*506T>A ENSP00000496202.1:n.*506T>A
ENST00000260682.6:c.*24T>A ENSP00000260682.6:n.*24T>A
NM_000771.3:c.*24T>A NP_000762.2:n.*24T>A
NM_000771.4:c.*24T>A MANE Select NP_000762.2:n.*24T>A