Canonical Allele Identifier: CA2645461962
Gene: FAAH HGNC NCBI

Linked Data

gnomAD v4: 1-46413819-C-A
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.46413819C>A , CM000663.2:g.46413819C>A GRCh38
NC_000001.10:g.46879491C>A , CM000663.1:g.46879491C>A GRCh37
NC_000001.9:g.46652078C>A NCBI36
NG_012195.1:g.24553C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000243167.9:c.*244C>A MANE Select ENSP00000243167.8:n.*244C>A
ENST00000243167.8:c.*244C>A ENSP00000243167.8:n.*244C>A
ENST00000484697.5:c.1017C>A
NM_001441.2:c.*244C>A NP_001432.2:n.*244C>A
NM_001441.3:c.*244C>A MANE Select NP_001432.2:n.*244C>A
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