Canonical Allele Identifier: CA182116694
Gene: CFAP418-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs569974676
gnomAD v2: 8-96515790-T-G
gnomAD v3: 8-95503562-T-G
gnomAD v4: 8-95503562-T-G

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.95503562T>G , CM000670.2:g.95503562T>G GRCh38
NC_000008.10:g.96515790T>G , CM000670.1:g.96515790T>G GRCh37
NC_000008.9:g.96584966T>G NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_038201.1:n.281+70782T>G
NR_038202.1:n.210+70782T>G
NR_038203.1:n.127-107102T>G
NR_038204.1:n.56-107102T>G
NR_038205.1:n.56-107102T>G
NR_038206.1:n.56-107102T>G
NR_038207.1:n.210+70782T>G
NR_038208.1:n.126+202370T>G
NR_038209.1:n.219-107102T>G