Canonical Allele Identifier: CA21919946
Gene: FAAH HGNC NCBI

Linked Data

dbSNP Id: rs767257628
gnomAD v4: 1-46413697-T-C
MyVariant Identifiers: chr1:g.46879369T>C (hg19) chr1:g.46413697T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.46413697T>C , CM000663.2:g.46413697T>C GRCh38
NC_000001.10:g.46879369T>C , CM000663.1:g.46879369T>C GRCh37
NC_000001.9:g.46651956T>C NCBI36
NG_012195.1:g.24431T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000243167.9:c.*122T>C MANE Select ENSP00000243167.8:n.*122T>C
ENST00000243167.8:c.*122T>C ENSP00000243167.8:n.*122T>C
ENST00000484697.5:c.895T>C
NM_001441.2:c.*122T>C NP_001432.2:n.*122T>C
NM_001441.3:c.*122T>C MANE Select NP_001432.2:n.*122T>C
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