Canonical Allele Identifier: CA522590791
Gene: FAAH HGNC NCBI

Linked Data

dbSNP Id: rs1344237134
gnomAD v2: 1-46865038-C-T
gnomAD v3: 1-46399366-C-T
gnomAD v4: 1-46399366-C-T
MyVariant Identifiers: chr1:g.46865038C>T (hg19) chr1:g.46399366C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.46399366C>T , CM000663.2:g.46399366C>T GRCh38
NC_000001.10:g.46865038C>T , CM000663.1:g.46865038C>T GRCh37
NC_000001.9:g.46637625C>T NCBI36
NG_012195.1:g.10100C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000243167.9:c.196-2725C>T MANE Select ENSP00000243167.8:n.196-2725C>T
ENST00000243167.8:c.196-2725C>T ENSP00000243167.8:n.196-2725C>T
ENST00000468718.5:n.216-2725C>T
ENST00000493735.5:n.174-2725C>T
NM_001441.2:c.196-2725C>T NP_001432.2:n.196-2725C>T
NM_001441.3:c.196-2725C>T MANE Select NP_001432.2:n.196-2725C>T
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