Canonical Allele Identifier: CA2474169138

Gene: FAAH

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.46399239T= , CM000663.2:g.46399239T=	GRCh38
NC_000001.10:g.46864911T= , CM000663.1:g.46864911T=	GRCh37
NC_000001.9:g.46637498T=	NCBI36
NG_012195.1:g.9973T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000243167.9:c.196-2852T= MANE Select	ENSP00000243167.8:n.196-2852T=
ENST00000243167.8:c.196-2852T=	ENSP00000243167.8:n.196-2852T=
ENST00000468718.5:n.216-2852T=
ENST00000493735.5:n.174-2852T=
NM_001441.2:c.196-2852T=	NP_001432.2:n.196-2852T=
NM_001441.3:c.196-2852T= MANE Select	NP_001432.2:n.196-2852T=