Canonical Allele Identifier: CA2645461823
Gene: FAAH HGNC NCBI

Linked Data

gnomAD v4: 1-46413705-C-G
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.46413705C>G , CM000663.2:g.46413705C>G GRCh38
NC_000001.10:g.46879377C>G , CM000663.1:g.46879377C>G GRCh37
NC_000001.9:g.46651964C>G NCBI36
NG_012195.1:g.24439C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000243167.9:c.*130C>G MANE Select ENSP00000243167.8:n.*130C>G
ENST00000243167.8:c.*130C>G ENSP00000243167.8:n.*130C>G
ENST00000484697.5:c.903C>G
NM_001441.2:c.*130C>G NP_001432.2:n.*130C>G
NM_001441.3:c.*130C>G MANE Select NP_001432.2:n.*130C>G
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