Canonical Allele Identifier: CA1116841752
Gene: CFAP418-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs1817075959
gnomAD v3: 8-95503539-C-T
gnomAD v4: 8-95503539-C-T
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.95503539C>T , CM000670.2:g.95503539C>T GRCh38
NC_000008.10:g.96515767C>T , CM000670.1:g.96515767C>T GRCh37
NC_000008.9:g.96584943C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_038201.1:n.281+70759C>T
NR_038202.1:n.210+70759C>T
NR_038203.1:n.127-107125C>T
NR_038204.1:n.56-107125C>T
NR_038205.1:n.56-107125C>T
NR_038206.1:n.56-107125C>T
NR_038207.1:n.210+70759C>T
NR_038208.1:n.126+202347C>T
NR_038209.1:n.219-107125C>T
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