Canonical Allele Identifier: CA2996915371
Gene: IFT43 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.75985692T>G , CM000676.2:g.75985692T>G GRCh38
NC_000014.8:g.76452035T>G , CM000676.1:g.76452035T>G GRCh37
NC_000014.7:g.75521788T>G NCBI36
NG_011715.1:g.1058A>C , LRG_399:g.1058A>C
NG_031957.1:g.4940T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000555677.5:n.90-3193T>G