Canonical Allele Identifier: CA2645461829
Gene: FAAH HGNC NCBI

Linked Data

gnomAD v4: 1-46413708-C-T
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.46413708C>T , CM000663.2:g.46413708C>T GRCh38
NC_000001.10:g.46879380C>T , CM000663.1:g.46879380C>T GRCh37
NC_000001.9:g.46651967C>T NCBI36
NG_012195.1:g.24442C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000243167.9:c.*133C>T MANE Select ENSP00000243167.8:n.*133C>T
ENST00000243167.8:c.*133C>T ENSP00000243167.8:n.*133C>T
ENST00000484697.5:c.906C>T
NM_001441.2:c.*133C>T NP_001432.2:n.*133C>T
NM_001441.3:c.*133C>T MANE Select NP_001432.2:n.*133C>T
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Search 100 bp 3'