Canonical Allele Identifier: CA2743463343
Gene: FAAH HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.46399278C>A , CM000663.2:g.46399278C>A GRCh38
NC_000001.10:g.46864950C>A , CM000663.1:g.46864950C>A GRCh37
NC_000001.9:g.46637537C>A NCBI36
NG_012195.1:g.10012C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000243167.9:c.196-2813C>A MANE Select ENSP00000243167.8:n.196-2813C>A
ENST00000243167.8:c.196-2813C>A ENSP00000243167.8:n.196-2813C>A
ENST00000468718.5:n.216-2813C>A
ENST00000493735.5:n.174-2813C>A
NM_001441.2:c.196-2813C>A NP_001432.2:n.196-2813C>A
NM_001441.3:c.196-2813C>A MANE Select NP_001432.2:n.196-2813C>A