Canonical Allele Identifier: CA736285611
Gene: FAAH HGNC NCBI

Linked Data

dbSNP Id: rs1241330020
gnomAD v3: 1-46399214-T-C
gnomAD v4: 1-46399214-T-C
MyVariant Identifiers: chr1:g.46864886T>C (hg19) chr1:g.46399214T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.46399214T>C , CM000663.2:g.46399214T>C GRCh38
NC_000001.10:g.46864886T>C , CM000663.1:g.46864886T>C GRCh37
NC_000001.9:g.46637473T>C NCBI36
NG_012195.1:g.9948T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000243167.9:c.196-2877T>C MANE Select ENSP00000243167.8:n.196-2877T>C
ENST00000243167.8:c.196-2877T>C ENSP00000243167.8:n.196-2877T>C
ENST00000468718.5:n.216-2877T>C
ENST00000493735.5:n.174-2877T>C
NM_001441.2:c.196-2877T>C NP_001432.2:n.196-2877T>C
NM_001441.3:c.196-2877T>C MANE Select NP_001432.2:n.196-2877T>C
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