Canonical Allele Identifier: CA2625774198
Gene: IFT43 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.75985691G>C , CM000676.2:g.75985691G>C GRCh38
NC_000014.8:g.76452034G>C , CM000676.1:g.76452034G>C GRCh37
NC_000014.7:g.75521787G>C NCBI36
NG_011715.1:g.1059C>G , LRG_399:g.1059C>G
NG_031957.1:g.4939G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000555677.5:n.90-3194G>C