Canonical Allele Identifier: CA2996915367
Gene: IFT43 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.75985688T>A , CM000676.2:g.75985688T>A GRCh38
NC_000014.8:g.76452031T>A , CM000676.1:g.76452031T>A GRCh37
NC_000014.7:g.75521784T>A NCBI36
NG_011715.1:g.1062A>T , LRG_399:g.1062A>T
NG_031957.1:g.4936T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000555677.5:n.90-3197T>A