Canonical Allele Identifier: CA2147731319
Gene: IFT43 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.75985695C= , CM000676.2:g.75985695C= GRCh38
NC_000014.8:g.76452038C= , CM000676.1:g.76452038C= GRCh37
NC_000014.7:g.75521791C= NCBI36
NG_011715.1:g.1055G= , LRG_399:g.1055G=
NG_031957.1:g.4943C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000555677.5:n.90-3190C=