Canonical Allele Identifier: CA2474169167
Gene: FAAH HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.46399308A= , CM000663.2:g.46399308A= GRCh38
NC_000001.10:g.46864980A= , CM000663.1:g.46864980A= GRCh37
NC_000001.9:g.46637567A= NCBI36
NG_012195.1:g.10042A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000243167.9:c.196-2783A= MANE Select ENSP00000243167.8:n.196-2783A=
ENST00000243167.8:c.196-2783A= ENSP00000243167.8:n.196-2783A=
ENST00000468718.5:n.216-2783A=
ENST00000493735.5:n.174-2783A=
NM_001441.2:c.196-2783A= NP_001432.2:n.196-2783A=
NM_001441.3:c.196-2783A= MANE Select NP_001432.2:n.196-2783A=
Search 100 bp 5'
Search 100 bp 3'