Canonical Allele Identifier: CA2743463811
Gene: FAAH HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.46413803T>C , CM000663.2:g.46413803T>C GRCh38
NC_000001.10:g.46879475T>C , CM000663.1:g.46879475T>C GRCh37
NC_000001.9:g.46652062T>C NCBI36
NG_012195.1:g.24537T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000243167.9:c.*228T>C MANE Select ENSP00000243167.8:n.*228T>C
ENST00000243167.8:c.*228T>C ENSP00000243167.8:n.*228T>C
ENST00000484697.5:c.1001T>C
NM_001441.2:c.*228T>C NP_001432.2:n.*228T>C
NM_001441.3:c.*228T>C MANE Select NP_001432.2:n.*228T>C
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