Canonical Allele Identifier: CA21931419
Gene: FAAH HGNC NCBI

Linked Data

dbSNP Id: rs1027667344
gnomAD v3: 1-46399253-T-G
gnomAD v4: 1-46399253-T-G
MyVariant Identifiers: chr1:g.46864925T>G (hg19) chr1:g.46399253T>G (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.46399253T>G , CM000663.2:g.46399253T>G GRCh38
NC_000001.10:g.46864925T>G , CM000663.1:g.46864925T>G GRCh37
NC_000001.9:g.46637512T>G NCBI36
NG_012195.1:g.9987T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000243167.9:c.196-2838T>G MANE Select ENSP00000243167.8:n.196-2838T>G
ENST00000243167.8:c.196-2838T>G ENSP00000243167.8:n.196-2838T>G
ENST00000468718.5:n.216-2838T>G
ENST00000493735.5:n.174-2838T>G
NM_001441.2:c.196-2838T>G NP_001432.2:n.196-2838T>G
NM_001441.3:c.196-2838T>G MANE Select NP_001432.2:n.196-2838T>G
Search 100 bp 5'
Search 100 bp 3'