Canonical Allele Identifier: CA2474169135
Gene: FAAH HGNC NCBI

Linked Data

dbSNP Id: rs535477976
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.46399228T>C , CM000663.2:g.46399228T>C GRCh38
NC_000001.10:g.46864900T>C , CM000663.1:g.46864900T>C GRCh37
NC_000001.9:g.46637487T>C NCBI36
NG_012195.1:g.9962T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000243167.9:c.196-2863T>C MANE Select ENSP00000243167.8:n.196-2863T>C
ENST00000243167.8:c.196-2863T>C ENSP00000243167.8:n.196-2863T>C
ENST00000468718.5:n.216-2863T>C
ENST00000493735.5:n.174-2863T>C
NM_001441.2:c.196-2863T>C NP_001432.2:n.196-2863T>C
NM_001441.3:c.196-2863T>C MANE Select NP_001432.2:n.196-2863T>C
Search 100 bp 5'
Search 100 bp 3'