Canonical Allele Identifier: CA2474169147

Gene: FAAH

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.46399254C= , CM000663.2:g.46399254C=	GRCh38
NC_000001.10:g.46864926C= , CM000663.1:g.46864926C=	GRCh37
NC_000001.9:g.46637513C=	NCBI36
NG_012195.1:g.9988C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000243167.9:c.196-2837C= MANE Select	ENSP00000243167.8:n.196-2837C=
ENST00000243167.8:c.196-2837C=	ENSP00000243167.8:n.196-2837C=
ENST00000468718.5:n.216-2837C=
ENST00000493735.5:n.174-2837C=
NM_001441.2:c.196-2837C=	NP_001432.2:n.196-2837C=
NM_001441.3:c.196-2837C= MANE Select	NP_001432.2:n.196-2837C=