Canonical Allele Identifier: CA2474175071
Gene: FAAH HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.46413696C= , CM000663.2:g.46413696C= GRCh38
NC_000001.10:g.46879368C= , CM000663.1:g.46879368C= GRCh37
NC_000001.9:g.46651955C= NCBI36
NG_012195.1:g.24430C=

Transcript Alleles

HGVS Amino-acid change
ENST00000243167.9:c.*121C= MANE Select ENSP00000243167.8:n.*121C=
ENST00000243167.8:c.*121C= ENSP00000243167.8:n.*121C=
ENST00000484697.5:c.894C=
NM_001441.2:c.*121C= NP_001432.2:n.*121C=
NM_001441.3:c.*121C= MANE Select NP_001432.2:n.*121C=