Canonical Allele Identifier: CA21931466
Gene: FAAH HGNC NCBI

Linked Data

dbSNP Id: rs1044638915
gnomAD v2: 1-46865080-T-C
gnomAD v3: 1-46399408-T-C
gnomAD v4: 1-46399408-T-C
MyVariant Identifiers: chr1:g.46865080T>C (hg19) chr1:g.46399408T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.46399408T>C , CM000663.2:g.46399408T>C GRCh38
NC_000001.10:g.46865080T>C , CM000663.1:g.46865080T>C GRCh37
NC_000001.9:g.46637667T>C NCBI36
NG_012195.1:g.10142T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000243167.9:c.196-2683T>C MANE Select ENSP00000243167.8:n.196-2683T>C
ENST00000243167.8:c.196-2683T>C ENSP00000243167.8:n.196-2683T>C
ENST00000468718.5:n.216-2683T>C
ENST00000493735.5:n.174-2683T>C
NM_001441.2:c.196-2683T>C NP_001432.2:n.196-2683T>C
NM_001441.3:c.196-2683T>C MANE Select NP_001432.2:n.196-2683T>C
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