Canonical Allele Identifier: CA182116696
Gene: CFAP418-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs909256416
gnomAD v3: 8-95503568-G-T
gnomAD v4: 8-95503568-G-T
MyVariant Identifiers: chr8:g.96515796G>T (hg19) chr8:g.95503568G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.95503568G>T , CM000670.2:g.95503568G>T GRCh38
NC_000008.10:g.96515796G>T , CM000670.1:g.96515796G>T GRCh37
NC_000008.9:g.96584972G>T NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_038201.1:n.281+70788G>T
NR_038202.1:n.210+70788G>T
NR_038203.1:n.127-107096G>T
NR_038204.1:n.56-107096G>T
NR_038205.1:n.56-107096G>T
NR_038206.1:n.56-107096G>T
NR_038207.1:n.210+70788G>T
NR_038208.1:n.126+202376G>T
NR_038209.1:n.219-107096G>T
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