Canonical Allele Identifier: CA2474175082
Gene: FAAH HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.46413715G= , CM000663.2:g.46413715G= GRCh38
NC_000001.10:g.46879387G= , CM000663.1:g.46879387G= GRCh37
NC_000001.9:g.46651974G= NCBI36
NG_012195.1:g.24449G=

Transcript Alleles

HGVS Amino-acid change
ENST00000243167.9:c.*140G= MANE Select ENSP00000243167.8:n.*140G=
ENST00000243167.8:c.*140G= ENSP00000243167.8:n.*140G=
ENST00000484697.5:c.913G=
NM_001441.2:c.*140G= NP_001432.2:n.*140G=
NM_001441.3:c.*140G= MANE Select NP_001432.2:n.*140G=