Canonical Allele Identifier: CA2474169181
Gene: FAAH HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.46399347C= , CM000663.2:g.46399347C= GRCh38
NC_000001.10:g.46865019C= , CM000663.1:g.46865019C= GRCh37
NC_000001.9:g.46637606C= NCBI36
NG_012195.1:g.10081C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000243167.9:c.196-2744C= MANE Select ENSP00000243167.8:n.196-2744C=
ENST00000243167.8:c.196-2744C= ENSP00000243167.8:n.196-2744C=
ENST00000468718.5:n.216-2744C=
ENST00000493735.5:n.174-2744C=
NM_001441.2:c.196-2744C= NP_001432.2:n.196-2744C=
NM_001441.3:c.196-2744C= MANE Select NP_001432.2:n.196-2744C=
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