Canonical Allele Identifier: CA857195323
Gene: CFAP418-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs1200090473
gnomAD v3: 8-95503506-T-C
gnomAD v4: 8-95503506-T-C

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.95503506T>C , CM000670.2:g.95503506T>C GRCh38
NC_000008.10:g.96515734T>C , CM000670.1:g.96515734T>C GRCh37
NC_000008.9:g.96584910T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_038201.1:n.281+70726T>C
NR_038202.1:n.210+70726T>C
NR_038203.1:n.127-107158T>C
NR_038204.1:n.56-107158T>C
NR_038205.1:n.56-107158T>C
NR_038206.1:n.56-107158T>C
NR_038207.1:n.210+70726T>C
NR_038208.1:n.126+202314T>C
NR_038209.1:n.219-107158T>C