Canonical Allele Identifier: CA736285642

Gene: FAAH

Linked Data

• dbSNP Id: rs1489901457
• MyVariant Identifiers: chr1:g.46864991C>T (hg19) ; chr1:g.46399319C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.46399319C>T , CM000663.2:g.46399319C>T	GRCh38
NC_000001.10:g.46864991C>T , CM000663.1:g.46864991C>T	GRCh37
NC_000001.9:g.46637578C>T	NCBI36
NG_012195.1:g.10053C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000243167.9:c.196-2772C>T MANE Select	ENSP00000243167.8:n.196-2772C>T
ENST00000243167.8:c.196-2772C>T	ENSP00000243167.8:n.196-2772C>T
ENST00000468718.5:n.216-2772C>T
ENST00000493735.5:n.174-2772C>T
NM_001441.2:c.196-2772C>T	NP_001432.2:n.196-2772C>T
NM_001441.3:c.196-2772C>T MANE Select	NP_001432.2:n.196-2772C>T