Canonical Allele Identifier: CA21931392
Gene: FAAH HGNC NCBI

Linked Data

dbSNP Id: rs776457125
gnomAD v2: 1-46864894-G-A
gnomAD v3: 1-46399222-G-A
gnomAD v4: 1-46399222-G-A
MyVariant Identifiers: chr1:g.46864894G>A (hg19) chr1:g.46399222G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.46399222G>A , CM000663.2:g.46399222G>A GRCh38
NC_000001.10:g.46864894G>A , CM000663.1:g.46864894G>A GRCh37
NC_000001.9:g.46637481G>A NCBI36
NG_012195.1:g.9956G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000243167.9:c.196-2869G>A MANE Select ENSP00000243167.8:n.196-2869G>A
ENST00000243167.8:c.196-2869G>A ENSP00000243167.8:n.196-2869G>A
ENST00000468718.5:n.216-2869G>A
ENST00000493735.5:n.174-2869G>A
NM_001441.2:c.196-2869G>A NP_001432.2:n.196-2869G>A
NM_001441.3:c.196-2869G>A MANE Select NP_001432.2:n.196-2869G>A
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