Canonical Allele Identifier: CA182116690

Gene: CFAP418-AS1

Linked Data

• dbSNP Id: rs1047152952
• gnomAD v3: 8-95503530-T-C
• gnomAD v4: 8-95503530-T-C
• MyVariant Identifiers: chr8:g.96515758T>C (hg19) ; chr8:g.95503530T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.95503530T>C , CM000670.2:g.95503530T>C	GRCh38
NC_000008.10:g.96515758T>C , CM000670.1:g.96515758T>C	GRCh37
NC_000008.9:g.96584934T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_038201.1:n.281+70750T>C
NR_038202.1:n.210+70750T>C
NR_038203.1:n.127-107134T>C
NR_038204.1:n.56-107134T>C
NR_038205.1:n.56-107134T>C
NR_038206.1:n.56-107134T>C
NR_038207.1:n.210+70750T>C
NR_038208.1:n.126+202338T>C
NR_038209.1:n.219-107134T>C