Canonical Allele Identifier: CA2147731312
Gene: IFT43 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.75985690C= , CM000676.2:g.75985690C= GRCh38
NC_000014.8:g.76452033C= , CM000676.1:g.76452033C= GRCh37
NC_000014.7:g.75521786C= NCBI36
NG_011715.1:g.1060G= , LRG_399:g.1060G=
NG_031957.1:g.4938C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000555677.5:n.90-3195C=