Canonical Allele Identifier: CA21919949
Gene: FAAH HGNC NCBI

Linked Data

dbSNP Id: rs779498182
MyVariant Identifiers: chr1:g.46879377C>A (hg19) chr1:g.46413705C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.46413705C>A , CM000663.2:g.46413705C>A GRCh38
NC_000001.10:g.46879377C>A , CM000663.1:g.46879377C>A GRCh37
NC_000001.9:g.46651964C>A NCBI36
NG_012195.1:g.24439C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000243167.9:c.*130C>A MANE Select ENSP00000243167.8:n.*130C>A
ENST00000243167.8:c.*130C>A ENSP00000243167.8:n.*130C>A
ENST00000484697.5:c.903C>A
NM_001441.2:c.*130C>A NP_001432.2:n.*130C>A
NM_001441.3:c.*130C>A MANE Select NP_001432.2:n.*130C>A
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