Canonical Allele Identifier: CA1929342154
Gene: CYP2C9 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94981309C= , CM000672.2:g.94981309C= GRCh38
NC_000010.10:g.96741066C= , CM000672.1:g.96741066C= GRCh37
NC_000010.9:g.96731056C= NCBI36
NG_008385.1:g.47652C=
NG_008385.2:g.48152C=

Transcript Alleles

HGVS Amino-acid change
ENST00000260682.8:c.1088C= MANE Select ENSP00000260682.6:p.Pro363=
ENST00000643112.1:c.*97C= ENSP00000496202.1:n.*97C=
ENST00000260682.6:c.1088C= ENSP00000260682.6:p.Pro363=
NM_000771.3:c.1088C= NP_000762.2:p.Pro363=
NM_000771.4:c.1088C= MANE Select NP_000762.2:p.Pro363=