Canonical Allele Identifier: CA2474169206
Gene: FAAH HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.46399421A= , CM000663.2:g.46399421A= GRCh38
NC_000001.10:g.46865093A= , CM000663.1:g.46865093A= GRCh37
NC_000001.9:g.46637680A= NCBI36
NG_012195.1:g.10155A=

Transcript Alleles

HGVS Amino-acid change
ENST00000243167.9:c.196-2670A= MANE Select ENSP00000243167.8:n.196-2670A=
ENST00000243167.8:c.196-2670A= ENSP00000243167.8:n.196-2670A=
ENST00000468718.5:n.216-2670A=
ENST00000493735.5:n.174-2670A=
NM_001441.2:c.196-2670A= NP_001432.2:n.196-2670A=
NM_001441.3:c.196-2670A= MANE Select NP_001432.2:n.196-2670A=