Canonical Allele Identifier: CA2841095556
Gene: IFT43 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.75985687C>T , CM000676.2:g.75985687C>T GRCh38
NC_000014.8:g.76452030C>T , CM000676.1:g.76452030C>T GRCh37
NC_000014.7:g.75521783C>T NCBI36
NG_011715.1:g.1063G>A , LRG_399:g.1063G>A
NG_031957.1:g.4935C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000555677.5:n.90-3198C>T