Canonical Allele Identifier: CA2645461965
Gene: FAAH HGNC NCBI

Linked Data

gnomAD v4: 1-46413821-A-G
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.46413821A>G , CM000663.2:g.46413821A>G GRCh38
NC_000001.10:g.46879493A>G , CM000663.1:g.46879493A>G GRCh37
NC_000001.9:g.46652080A>G NCBI36
NG_012195.1:g.24555A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000243167.9:c.*246A>G MANE Select ENSP00000243167.8:n.*246A>G
ENST00000243167.8:c.*246A>G ENSP00000243167.8:n.*246A>G
ENST00000484697.5:c.1019A>G
NM_001441.2:c.*246A>G NP_001432.2:n.*246A>G
NM_001441.3:c.*246A>G MANE Select NP_001432.2:n.*246A>G
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