Canonical Allele Identifier: CA522590784

Gene: FAAH

Linked Data

• dbSNP Id: rs1388766163
• gnomAD v2: 1-46865003-C-T
• gnomAD v3: 1-46399331-C-T
• gnomAD v4: 1-46399331-C-T
• MyVariant Identifiers: chr1:g.46865003C>T (hg19) ; chr1:g.46399331C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.46399331C>T , CM000663.2:g.46399331C>T	GRCh38
NC_000001.10:g.46865003C>T , CM000663.1:g.46865003C>T	GRCh37
NC_000001.9:g.46637590C>T	NCBI36
NG_012195.1:g.10065C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000243167.9:c.196-2760C>T MANE Select	ENSP00000243167.8:n.196-2760C>T
ENST00000243167.8:c.196-2760C>T	ENSP00000243167.8:n.196-2760C>T
ENST00000468718.5:n.216-2760C>T
ENST00000493735.5:n.174-2760C>T
NM_001441.2:c.196-2760C>T	NP_001432.2:n.196-2760C>T
NM_001441.3:c.196-2760C>T MANE Select	NP_001432.2:n.196-2760C>T