Canonical Allele Identifier: CA2147731326
Gene: IFT43 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.75985714A= , CM000676.2:g.75985714A= GRCh38
NC_000014.8:g.76452057A= , CM000676.1:g.76452057A= GRCh37
NC_000014.7:g.75521810A= NCBI36
NG_011715.1:g.1036T= , LRG_399:g.1036T=
NG_031957.1:g.4962A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000555677.5:n.90-3171A=