Canonical Allele Identifier: CA2474169188

Gene: FAAH

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.46399363G= , CM000663.2:g.46399363G=	GRCh38
NC_000001.10:g.46865035G= , CM000663.1:g.46865035G=	GRCh37
NC_000001.9:g.46637622G=	NCBI36
NG_012195.1:g.10097G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000243167.9:c.196-2728G= MANE Select	ENSP00000243167.8:n.196-2728G=
ENST00000243167.8:c.196-2728G=	ENSP00000243167.8:n.196-2728G=
ENST00000468718.5:n.216-2728G=
ENST00000493735.5:n.174-2728G=
NM_001441.2:c.196-2728G=	NP_001432.2:n.196-2728G=
NM_001441.3:c.196-2728G= MANE Select	NP_001432.2:n.196-2728G=