Canonical Allele Identifier: CA583717735
Gene: CFAP418-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs1437022762
gnomAD v2: 8-96515836-C-G
gnomAD v3: 8-95503608-C-G
gnomAD v4: 8-95503608-C-G
MyVariant Identifiers: chr8:g.96515836C>G (hg19) chr8:g.95503608C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.95503608C>G , CM000670.2:g.95503608C>G GRCh38
NC_000008.10:g.96515836C>G , CM000670.1:g.96515836C>G GRCh37
NC_000008.9:g.96585012C>G NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_038201.1:n.281+70828C>G
NR_038202.1:n.210+70828C>G
NR_038203.1:n.127-107056C>G
NR_038204.1:n.56-107056C>G
NR_038205.1:n.56-107056C>G
NR_038206.1:n.56-107056C>G
NR_038207.1:n.210+70828C>G
NR_038208.1:n.126+202416C>G
NR_038209.1:n.219-107056C>G
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