Canonical Allele Identifier: CA2625774201
Gene: IFT43 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.75985693A>T , CM000676.2:g.75985693A>T GRCh38
NC_000014.8:g.76452036A>T , CM000676.1:g.76452036A>T GRCh37
NC_000014.7:g.75521789A>T NCBI36
NG_011715.1:g.1057T>A , LRG_399:g.1057T>A
NG_031957.1:g.4941A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000555677.5:n.90-3192A>T