Canonical Allele Identifier: CA2147731317
Gene: IFT43 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.75985694C= , CM000676.2:g.75985694C= GRCh38
NC_000014.8:g.76452037C= , CM000676.1:g.76452037C= GRCh37
NC_000014.7:g.75521790C= NCBI36
NG_011715.1:g.1056G= , LRG_399:g.1056G=
NG_031957.1:g.4942C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000555677.5:n.90-3191C=