Canonical Allele Identifier: CA915669471
Gene: CFAP418-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs1563591184
gnomAD v2: 8-96515813-C-T
gnomAD v3: 8-95503585-C-T
gnomAD v4: 8-95503585-C-T

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.95503585C>T , CM000670.2:g.95503585C>T GRCh38
NC_000008.10:g.96515813C>T , CM000670.1:g.96515813C>T GRCh37
NC_000008.9:g.96584989C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_038201.1:n.281+70805C>T
NR_038202.1:n.210+70805C>T
NR_038203.1:n.127-107079C>T
NR_038204.1:n.56-107079C>T
NR_038205.1:n.56-107079C>T
NR_038206.1:n.56-107079C>T
NR_038207.1:n.210+70805C>T
NR_038208.1:n.126+202393C>T
NR_038209.1:n.219-107079C>T