Canonical Allele Identifier: CA2474169217
Gene: FAAH HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.46399453C= , CM000663.2:g.46399453C= GRCh38
NC_000001.10:g.46865125C= , CM000663.1:g.46865125C= GRCh37
NC_000001.9:g.46637712C= NCBI36
NG_012195.1:g.10187C=

Transcript Alleles

HGVS Amino-acid change
ENST00000243167.9:c.196-2638C= MANE Select ENSP00000243167.8:n.196-2638C=
ENST00000243167.8:c.196-2638C= ENSP00000243167.8:n.196-2638C=
ENST00000468718.5:n.216-2638C=
ENST00000493735.5:n.174-2638C=
NM_001441.2:c.196-2638C= NP_001432.2:n.196-2638C=
NM_001441.3:c.196-2638C= MANE Select NP_001432.2:n.196-2638C=