Canonical Allele Identifier: CA2474175077
Gene: FAAH HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.46413705C= , CM000663.2:g.46413705C= GRCh38
NC_000001.10:g.46879377C= , CM000663.1:g.46879377C= GRCh37
NC_000001.9:g.46651964C= NCBI36
NG_012195.1:g.24439C=

Transcript Alleles

HGVS Amino-acid change
ENST00000243167.9:c.*130C= MANE Select ENSP00000243167.8:n.*130C=
ENST00000243167.8:c.*130C= ENSP00000243167.8:n.*130C=
ENST00000484697.5:c.903C=
NM_001441.2:c.*130C= NP_001432.2:n.*130C=
NM_001441.3:c.*130C= MANE Select NP_001432.2:n.*130C=