Canonical Allele Identifier: CA2474175080
Gene: FAAH HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.46413710T= , CM000663.2:g.46413710T= GRCh38
NC_000001.10:g.46879382T= , CM000663.1:g.46879382T= GRCh37
NC_000001.9:g.46651969T= NCBI36
NG_012195.1:g.24444T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000243167.9:c.*135T= MANE Select ENSP00000243167.8:n.*135T=
ENST00000243167.8:c.*135T= ENSP00000243167.8:n.*135T=
ENST00000484697.5:c.908T=
NM_001441.2:c.*135T= NP_001432.2:n.*135T=
NM_001441.3:c.*135T= MANE Select NP_001432.2:n.*135T=