Canonical Allele Identifier: CA2625774194
Gene: IFT43 HGNC NCBI

Linked Data

Genomic Alleles

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

Transcript Alleles

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