Canonical Allele Identifier: CA736285652
Gene: FAAH HGNC NCBI

Linked Data

dbSNP Id: rs1344237134
MyVariant Identifiers: chr1:g.46865038C>A (hg19) chr1:g.46399366C>A (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.46399366C>A , CM000663.2:g.46399366C>A GRCh38
NC_000001.10:g.46865038C>A , CM000663.1:g.46865038C>A GRCh37
NC_000001.9:g.46637625C>A NCBI36
NG_012195.1:g.10100C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000243167.9:c.196-2725C>A MANE Select ENSP00000243167.8:n.196-2725C>A
ENST00000243167.8:c.196-2725C>A ENSP00000243167.8:n.196-2725C>A
ENST00000468718.5:n.216-2725C>A
ENST00000493735.5:n.174-2725C>A
NM_001441.2:c.196-2725C>A NP_001432.2:n.196-2725C>A
NM_001441.3:c.196-2725C>A MANE Select NP_001432.2:n.196-2725C>A
Search 100 bp 5'
Search 100 bp 3'