Canonical Allele Identifier: CA1001316076
Gene: FAAH HGNC NCBI

Linked Data

dbSNP Id: rs1228001311
gnomAD v3: 1-46399189-G-A
gnomAD v4: 1-46399189-G-A
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.46399189G>A , CM000663.2:g.46399189G>A GRCh38
NC_000001.10:g.46864861G>A , CM000663.1:g.46864861G>A GRCh37
NC_000001.9:g.46637448G>A NCBI36
NG_012195.1:g.9923G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000243167.9:c.196-2902G>A MANE Select ENSP00000243167.8:n.196-2902G>A
ENST00000243167.8:c.196-2902G>A ENSP00000243167.8:n.196-2902G>A
ENST00000468718.5:n.216-2902G>A
ENST00000493735.5:n.174-2902G>A
NM_001441.2:c.196-2902G>A NP_001432.2:n.196-2902G>A
NM_001441.3:c.196-2902G>A MANE Select NP_001432.2:n.196-2902G>A
Search 100 bp 5'
Search 100 bp 3'