Canonical Allele Identifier: CA21931381
Gene: FAAH HGNC NCBI

Linked Data

dbSNP Id: rs905845227
gnomAD v3: 1-46399192-CAGA-C
gnomAD v4: 1-46399192-CAGA-C
MyVariant Identifiers: chr1:g.46864865_46864867del (hg19) chr1:g.46399193_46399195del (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.46399195_46399197del , CM000663.2:g.46399195_46399197del GRCh38
NC_000001.10:g.46864867_46864869del , CM000663.1:g.46864867_46864869del GRCh37
NC_000001.9:g.46637454_46637456del NCBI36
NG_012195.1:g.9929_9931del

Transcript Alleles

HGVS Amino-acid Change
ENST00000243167.9:c.196-2896_196-2894del MANE Select ENSP00000243167.8:n.196-2896_196-2894del
ENST00000243167.8:c.196-2896_196-2894del ENSP00000243167.8:n.196-2896_196-2894del
ENST00000468718.5:n.216-2896_216-2894del
ENST00000493735.5:n.174-2896_174-2894del
NM_001441.2:c.196-2896_196-2894del NP_001432.2:n.196-2896_196-2894del
NM_001441.3:c.196-2896_196-2894del MANE Select NP_001432.2:n.196-2896_196-2894del
Search 100 bp 5'
Search 100 bp 3'