Canonical Allele Identifier: CA21931464
Gene: FAAH HGNC NCBI

Linked Data

dbSNP Id: rs950389321
gnomAD v2: 1-46865077-A-G
gnomAD v3: 1-46399405-A-G
gnomAD v4: 1-46399405-A-G

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.46399405A>G , CM000663.2:g.46399405A>G GRCh38
NC_000001.10:g.46865077A>G , CM000663.1:g.46865077A>G GRCh37
NC_000001.9:g.46637664A>G NCBI36
NG_012195.1:g.10139A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000243167.9:c.196-2686A>G MANE Select ENSP00000243167.8:n.196-2686A>G
ENST00000243167.8:c.196-2686A>G ENSP00000243167.8:n.196-2686A>G
ENST00000468718.5:n.216-2686A>G
ENST00000493735.5:n.174-2686A>G
NM_001441.2:c.196-2686A>G NP_001432.2:n.196-2686A>G
NM_001441.3:c.196-2686A>G MANE Select NP_001432.2:n.196-2686A>G