Canonical Allele Identifier: CA2474175081
Gene: FAAH HGNC NCBI

Linked Data

dbSNP Id: rs1664959177
gnomAD v4: 1-46413710-T-G
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.46413710T>G , CM000663.2:g.46413710T>G GRCh38
NC_000001.10:g.46879382T>G , CM000663.1:g.46879382T>G GRCh37
NC_000001.9:g.46651969T>G NCBI36
NG_012195.1:g.24444T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000243167.9:c.*135T>G MANE Select ENSP00000243167.8:n.*135T>G
ENST00000243167.8:c.*135T>G ENSP00000243167.8:n.*135T>G
ENST00000484697.5:c.908T>G
NM_001441.2:c.*135T>G NP_001432.2:n.*135T>G
NM_001441.3:c.*135T>G MANE Select NP_001432.2:n.*135T>G
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