Canonical Allele Identifier: CA1929349866
Gene: CYP2C9 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94989076T= , CM000672.2:g.94989076T= GRCh38
NC_000010.10:g.96748833T= , CM000672.1:g.96748833T= GRCh37
NC_000010.9:g.96738823T= NCBI36
NG_008385.1:g.55419T=
NG_008385.2:g.55919T=

Transcript Alleles

HGVS Amino-acid change
ENST00000260682.8:c.*48T= MANE Select ENSP00000260682.6:n.*48T=
ENST00000643112.1:c.*530T= ENSP00000496202.1:n.*530T=
ENST00000260682.6:c.*48T= ENSP00000260682.6:n.*48T=
NM_000771.3:c.*48T= NP_000762.2:n.*48T=
NM_000771.4:c.*48T= MANE Select NP_000762.2:n.*48T=