Canonical Allele Identifier: CA2474169133
Gene: FAAH HGNC NCBI

Linked Data

dbSNP Id: rs1664654448
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.46399225del , CM000663.2:g.46399225del GRCh38
NC_000001.10:g.46864897del , CM000663.1:g.46864897del GRCh37
NC_000001.9:g.46637484del NCBI36
NG_012195.1:g.9959del

Transcript Alleles

HGVS Amino-acid change
ENST00000243167.9:c.196-2866del MANE Select ENSP00000243167.8:n.196-2866del
ENST00000243167.8:c.196-2866del ENSP00000243167.8:n.196-2866del
ENST00000468718.5:n.216-2866del
ENST00000493735.5:n.174-2866del
NM_001441.2:c.196-2866del NP_001432.2:n.196-2866del
NM_001441.3:c.196-2866del MANE Select NP_001432.2:n.196-2866del
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Search 100 bp 3'