Canonical Allele Identifier: CA736285662

Gene: FAAH

Linked Data

• dbSNP Id: rs1485680513
• MyVariant Identifiers: chr1:g.46865114A>G (hg19) ; chr1:g.46399442A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.46399442A>G , CM000663.2:g.46399442A>G	GRCh38
NC_000001.10:g.46865114A>G , CM000663.1:g.46865114A>G	GRCh37
NC_000001.9:g.46637701A>G	NCBI36
NG_012195.1:g.10176A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000243167.9:c.196-2649A>G MANE Select	ENSP00000243167.8:n.196-2649A>G
ENST00000243167.8:c.196-2649A>G	ENSP00000243167.8:n.196-2649A>G
ENST00000468718.5:n.216-2649A>G
ENST00000493735.5:n.174-2649A>G
NM_001441.2:c.196-2649A>G	NP_001432.2:n.196-2649A>G
NM_001441.3:c.196-2649A>G MANE Select	NP_001432.2:n.196-2649A>G