Canonical Allele Identifier: CA340193819
Gene: FAAH HGNC NCBI

Linked Data

dbSNP Id: rs324419
MyVariant Identifiers: chr1:g.46871986T>A (hg19) chr1:g.46406314T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.46406314T>A , CM000663.2:g.46406314T>A GRCh38
NC_000001.10:g.46871986T>A , CM000663.1:g.46871986T>A GRCh37
NC_000001.9:g.46644573T>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000243167.9:c.897T>A MANE Select ENSP00000243167.8:p.Cys299Ter
ENST00000243167.8:c.897T>A ENSP00000243167.8:p.Cys299Ter
ENST00000484697.5:c.72+520T>A
ENST00000489366.2:n.112T>A
ENST00000493735.5:n.1118T>A
NM_001441.3:c.897T>A MANE Select NP_001432.2:p.Cys299Ter
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