Canonical Allele Identifier: CA2474169176
Gene: FAAH HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.46399331C= , CM000663.2:g.46399331C= GRCh38
NC_000001.10:g.46865003C= , CM000663.1:g.46865003C= GRCh37
NC_000001.9:g.46637590C= NCBI36
NG_012195.1:g.10065C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000243167.9:c.196-2760C= MANE Select ENSP00000243167.8:n.196-2760C=
ENST00000243167.8:c.196-2760C= ENSP00000243167.8:n.196-2760C=
ENST00000468718.5:n.216-2760C=
ENST00000493735.5:n.174-2760C=
NM_001441.2:c.196-2760C= NP_001432.2:n.196-2760C=
NM_001441.3:c.196-2760C= MANE Select NP_001432.2:n.196-2760C=
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