Canonical Allele Identifier: CA522590780
Gene: FAAH HGNC NCBI

Linked Data

dbSNP Id: rs1372474078
gnomAD v2: 1-46864927-C-T
gnomAD v3: 1-46399255-C-T
gnomAD v4: 1-46399255-C-T
MyVariant Identifiers: chr1:g.46864927C>T (hg19) chr1:g.46399255C>T (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.46399255C>T , CM000663.2:g.46399255C>T GRCh38
NC_000001.10:g.46864927C>T , CM000663.1:g.46864927C>T GRCh37
NC_000001.9:g.46637514C>T NCBI36
NG_012195.1:g.9989C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000243167.9:c.196-2836C>T MANE Select ENSP00000243167.8:n.196-2836C>T
ENST00000243167.8:c.196-2836C>T ENSP00000243167.8:n.196-2836C>T
ENST00000468718.5:n.216-2836C>T
ENST00000493735.5:n.174-2836C>T
NM_001441.2:c.196-2836C>T NP_001432.2:n.196-2836C>T
NM_001441.3:c.196-2836C>T MANE Select NP_001432.2:n.196-2836C>T
Search 100 bp 5'
Search 100 bp 3'