Canonical Allele Identifier: CA736229149
Gene: FAAH HGNC NCBI

Linked Data

dbSNP Id: rs1409338939
gnomAD v3: 1-46413719-C-T
gnomAD v4: 1-46413719-C-T
MyVariant Identifiers: chr1:g.46879391C>T (hg19) chr1:g.46413719C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.46413719C>T , CM000663.2:g.46413719C>T GRCh38
NC_000001.10:g.46879391C>T , CM000663.1:g.46879391C>T GRCh37
NC_000001.9:g.46651978C>T NCBI36
NG_012195.1:g.24453C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000243167.9:c.*144C>T MANE Select ENSP00000243167.8:n.*144C>T
ENST00000243167.8:c.*144C>T ENSP00000243167.8:n.*144C>T
ENST00000484697.5:c.917C>T
NM_001441.2:c.*144C>T NP_001432.2:n.*144C>T
NM_001441.3:c.*144C>T MANE Select NP_001432.2:n.*144C>T
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