Canonical Allele Identifier: CA2645461961
Gene: FAAH HGNC NCBI

Linked Data

gnomAD v4: 1-46413818-C-G
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.46413818C>G , CM000663.2:g.46413818C>G GRCh38
NC_000001.10:g.46879490C>G , CM000663.1:g.46879490C>G GRCh37
NC_000001.9:g.46652077C>G NCBI36
NG_012195.1:g.24552C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000243167.9:c.*243C>G MANE Select ENSP00000243167.8:n.*243C>G
ENST00000243167.8:c.*243C>G ENSP00000243167.8:n.*243C>G
ENST00000484697.5:c.1016C>G
NM_001441.2:c.*243C>G NP_001432.2:n.*243C>G
NM_001441.3:c.*243C>G MANE Select NP_001432.2:n.*243C>G
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