Canonical Allele Identifier: CA2474175072
Gene: FAAH HGNC NCBI

Linked Data

dbSNP Id: rs1664958691
gnomAD v4: 1-46413696-C-T
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.46413696C>T , CM000663.2:g.46413696C>T GRCh38
NC_000001.10:g.46879368C>T , CM000663.1:g.46879368C>T GRCh37
NC_000001.9:g.46651955C>T NCBI36
NG_012195.1:g.24430C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000243167.9:c.*121C>T MANE Select ENSP00000243167.8:n.*121C>T
ENST00000243167.8:c.*121C>T ENSP00000243167.8:n.*121C>T
ENST00000484697.5:c.894C>T
NM_001441.2:c.*121C>T NP_001432.2:n.*121C>T
NM_001441.3:c.*121C>T MANE Select NP_001432.2:n.*121C>T
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Search 100 bp 3'