Canonical Allele Identifier: CA2474169193
Gene: FAAH HGNC NCBI

Linked Data

dbSNP Id: rs917414340

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.46399370T>A , CM000663.2:g.46399370T>A GRCh38
NC_000001.10:g.46865042T>A , CM000663.1:g.46865042T>A GRCh37
NC_000001.9:g.46637629T>A NCBI36
NG_012195.1:g.10104T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000243167.9:c.196-2721T>A MANE Select ENSP00000243167.8:n.196-2721T>A
ENST00000243167.8:c.196-2721T>A ENSP00000243167.8:n.196-2721T>A
ENST00000468718.5:n.216-2721T>A
ENST00000493735.5:n.174-2721T>A
NM_001441.2:c.196-2721T>A NP_001432.2:n.196-2721T>A
NM_001441.3:c.196-2721T>A MANE Select NP_001432.2:n.196-2721T>A