Canonical Allele Identifier: CA736285649
Gene: FAAH HGNC NCBI

Linked Data

dbSNP Id: rs1402564973
gnomAD v3: 1-46399363-G-C
gnomAD v4: 1-46399363-G-C
MyVariant Identifiers: chr1:g.46865035G>C (hg19) chr1:g.46399363G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.46399363G>C , CM000663.2:g.46399363G>C GRCh38
NC_000001.10:g.46865035G>C , CM000663.1:g.46865035G>C GRCh37
NC_000001.9:g.46637622G>C NCBI36
NG_012195.1:g.10097G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000243167.9:c.196-2728G>C MANE Select ENSP00000243167.8:n.196-2728G>C
ENST00000243167.8:c.196-2728G>C ENSP00000243167.8:n.196-2728G>C
ENST00000468718.5:n.216-2728G>C
ENST00000493735.5:n.174-2728G>C
NM_001441.2:c.196-2728G>C NP_001432.2:n.196-2728G>C
NM_001441.3:c.196-2728G>C MANE Select NP_001432.2:n.196-2728G>C
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