Canonical Allele Identifier: CA736229141
Gene: FAAH HGNC NCBI

Linked Data

dbSNP Id: rs1328007564
gnomAD v3: 1-46413704-A-G
gnomAD v4: 1-46413704-A-G
MyVariant Identifiers: chr1:g.46879376A>G (hg19) chr1:g.46413704A>G (hg38)
JSON-LD

Genomic Alleles

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

Transcript Alleles

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