Canonical Allele Identifier: CA21931441

Gene: FAAH

Linked Data

• dbSNP Id: rs544946460
• gnomAD v2: 1-46865015-T-C
• gnomAD v3: 1-46399343-T-C
• gnomAD v4: 1-46399343-T-C
• MyVariant Identifiers: chr1:g.46865015T>C (hg19) ; chr1:g.46399343T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.46399343T>C , CM000663.2:g.46399343T>C	GRCh38
NC_000001.10:g.46865015T>C , CM000663.1:g.46865015T>C	GRCh37
NC_000001.9:g.46637602T>C	NCBI36
NG_012195.1:g.10077T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000243167.9:c.196-2748T>C MANE Select	ENSP00000243167.8:n.196-2748T>C
ENST00000243167.8:c.196-2748T>C	ENSP00000243167.8:n.196-2748T>C
ENST00000468718.5:n.216-2748T>C
ENST00000493735.5:n.174-2748T>C
NM_001441.2:c.196-2748T>C	NP_001432.2:n.196-2748T>C
NM_001441.3:c.196-2748T>C MANE Select	NP_001432.2:n.196-2748T>C