Canonical Allele Identifier: CA2147731318
Gene: IFT43 HGNC NCBI

Linked Data

dbSNP Id: rs2035502920
gnomAD v4: 14-75985694-C-A
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.75985694C>A , CM000676.2:g.75985694C>A GRCh38
NC_000014.8:g.76452037C>A , CM000676.1:g.76452037C>A GRCh37
NC_000014.7:g.75521790C>A NCBI36
NG_011715.1:g.1056G>T , LRG_399:g.1056G>T
NG_031957.1:g.4942C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000555677.5:n.90-3191C>A
Search 100 bp 5'
Search 100 bp 3'