Canonical Allele Identifier: CA5617425
Gene: CYP2C9 HGNC NCBI

Linked Data

dbSNP Id: rs774423253

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94989030G>A , CM000672.2:g.94989030G>A GRCh38
NC_000010.10:g.96748787G>A , CM000672.1:g.96748787G>A GRCh37
NC_000010.9:g.96738777G>A NCBI36
NG_008385.1:g.55373G>A
NG_008385.2:g.55873G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000260682.8:c.*2G>A MANE Select ENSP00000260682.6:n.*2G>A
ENST00000643112.1:c.*484G>A ENSP00000496202.1:n.*484G>A
ENST00000260682.6:c.*2G>A ENSP00000260682.6:n.*2G>A
NM_000771.3:c.*2G>A NP_000762.2:n.*2G>A
NM_000771.4:c.*2G>A MANE Select NP_000762.2:n.*2G>A