Canonical Allele Identifier: CA182116697
Gene: CFAP418-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs895097250
MyVariant Identifiers: chr8:g.95503570C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.95503570C>T , CM000670.2:g.95503570C>T GRCh38
NC_000008.10:g.96515798C>T , CM000670.1:g.96515798C>T GRCh37
NC_000008.9:g.96584974C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_038201.1:n.281+70790C>T
NR_038202.1:n.210+70790C>T
NR_038203.1:n.127-107094C>T
NR_038204.1:n.56-107094C>T
NR_038205.1:n.56-107094C>T
NR_038206.1:n.56-107094C>T
NR_038207.1:n.210+70790C>T
NR_038208.1:n.126+202378C>T
NR_038209.1:n.219-107094C>T
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