Canonical Allele Identifier: CA1929349840
Gene: CYP2C9 HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94989032A= , CM000672.2:g.94989032A= GRCh38
NC_000010.10:g.96748789A= , CM000672.1:g.96748789A= GRCh37
NC_000010.9:g.96738779A= NCBI36
NG_008385.1:g.55375A=
NG_008385.2:g.55875A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000260682.8:c.*4A= MANE Select ENSP00000260682.6:n.*4A=
ENST00000643112.1:c.*486A= ENSP00000496202.1:n.*486A=
ENST00000260682.6:c.*4A= ENSP00000260682.6:n.*4A=
NM_000771.3:c.*4A= NP_000762.2:n.*4A=
NM_000771.4:c.*4A= MANE Select NP_000762.2:n.*4A=
Search 100 bp 5'
Search 100 bp 3'