Canonical Allele Identifier: CA2996915369
Gene: IFT43 HGNC NCBI

Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid Change
ENST00000555677.5:n.90-3196G>A