Canonical Allele Identifier: CA964849696
Gene: IFT43 HGNC NCBI

Linked Data

dbSNP Id: rs2035502693

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.75985689del , CM000676.2:g.75985689del GRCh38
NC_000014.8:g.76452032del , CM000676.1:g.76452032del GRCh37
NC_000014.7:g.75521785del NCBI36
NG_011715.1:g.1061del , LRG_399:g.1061del
NG_031957.1:g.4937del

Transcript Alleles

HGVS Amino-acid Change
ENST00000555677.5:n.90-3196del