Canonical Allele Identifier: CA736285621
Gene: FAAH HGNC NCBI

Linked Data

dbSNP Id: rs1349998886
MyVariant Identifiers: chr1:g.46864913del (hg19) chr1:g.46399241del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.46399241del , CM000663.2:g.46399241del GRCh38
NC_000001.10:g.46864913del , CM000663.1:g.46864913del GRCh37
NC_000001.9:g.46637500del NCBI36
NG_012195.1:g.9975del

Transcript Alleles

HGVS Amino-acid Change
ENST00000243167.9:c.196-2850del MANE Select ENSP00000243167.8:n.196-2850del
ENST00000243167.8:c.196-2850del ENSP00000243167.8:n.196-2850del
ENST00000468718.5:n.216-2850del
ENST00000493735.5:n.174-2850del
NM_001441.2:c.196-2850del NP_001432.2:n.196-2850del
NM_001441.3:c.196-2850del MANE Select NP_001432.2:n.196-2850del
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