Canonical Allele Identifier: CA182116701
Gene: CFAP418-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs149953411
gnomAD v2: 8-96515843-G-A
gnomAD v3: 8-95503615-G-A
gnomAD v4: 8-95503615-G-A
MyVariant Identifiers: chr8:g.96515843G>A (hg19) chr8:g.95503615G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.95503615G>A , CM000670.2:g.95503615G>A GRCh38
NC_000008.10:g.96515843G>A , CM000670.1:g.96515843G>A GRCh37
NC_000008.9:g.96585019G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_038201.1:n.281+70835G>A
NR_038202.1:n.210+70835G>A
NR_038203.1:n.127-107049G>A
NR_038204.1:n.56-107049G>A
NR_038205.1:n.56-107049G>A
NR_038206.1:n.56-107049G>A
NR_038207.1:n.210+70835G>A
NR_038208.1:n.126+202423G>A
NR_038209.1:n.219-107049G>A
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