Canonical Allele Identifier: CA1147644881

Gene: FAAH

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.46399238G= , CM000663.2:g.46399238G=	GRCh38
NC_000001.10:g.46864910G= , CM000663.1:g.46864910G=	GRCh37
NC_000001.9:g.46637497G=	NCBI36
NG_012195.1:g.9972G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000243167.9:c.196-2853G= MANE Select	ENSP00000243167.8:n.196-2853G=
ENST00000243167.8:c.196-2853G=	ENSP00000243167.8:n.196-2853G=
ENST00000468718.5:n.216-2853G=
ENST00000493735.5:n.174-2853G=
NM_001441.2:c.196-2853G=	NP_001432.2:n.196-2853G=
NM_001441.3:c.196-2853G= MANE Select	NP_001432.2:n.196-2853G=