Canonical Allele Identifier: CA2645461820
Gene: FAAH HGNC NCBI

Linked Data

gnomAD v4: 1-46413704-A-C
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.46413704A>C , CM000663.2:g.46413704A>C GRCh38
NC_000001.10:g.46879376A>C , CM000663.1:g.46879376A>C GRCh37
NC_000001.9:g.46651963A>C NCBI36
NG_012195.1:g.24438A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000243167.9:c.*129A>C MANE Select ENSP00000243167.8:n.*129A>C
ENST00000243167.8:c.*129A>C ENSP00000243167.8:n.*129A>C
ENST00000484697.5:c.902A>C
NM_001441.2:c.*129A>C NP_001432.2:n.*129A>C
NM_001441.3:c.*129A>C MANE Select NP_001432.2:n.*129A>C
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Search 100 bp 3'