Canonical Allele Identifier: CA2474175127
Gene: FAAH HGNC NCBI

Linked Data

dbSNP Id: rs1664961100
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.46413819C>T , CM000663.2:g.46413819C>T GRCh38
NC_000001.10:g.46879491C>T , CM000663.1:g.46879491C>T GRCh37
NC_000001.9:g.46652078C>T NCBI36
NG_012195.1:g.24553C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000243167.9:c.*244C>T MANE Select ENSP00000243167.8:n.*244C>T
ENST00000243167.8:c.*244C>T ENSP00000243167.8:n.*244C>T
ENST00000484697.5:c.1017C>T
NM_001441.2:c.*244C>T NP_001432.2:n.*244C>T
NM_001441.3:c.*244C>T MANE Select NP_001432.2:n.*244C>T
Search 100 bp 5'
Search 100 bp 3'