Canonical Allele Identifier: CA2474169204
Gene: FAAH HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.46399410T= , CM000663.2:g.46399410T= GRCh38
NC_000001.10:g.46865082T= , CM000663.1:g.46865082T= GRCh37
NC_000001.9:g.46637669T= NCBI36
NG_012195.1:g.10144T=

Transcript Alleles

HGVS Amino-acid change
ENST00000243167.9:c.196-2681T= MANE Select ENSP00000243167.8:n.196-2681T=
ENST00000243167.8:c.196-2681T= ENSP00000243167.8:n.196-2681T=
ENST00000468718.5:n.216-2681T=
ENST00000493735.5:n.174-2681T=
NM_001441.2:c.196-2681T= NP_001432.2:n.196-2681T=
NM_001441.3:c.196-2681T= MANE Select NP_001432.2:n.196-2681T=