Canonical Allele Identifier: CA2147731322
Gene: IFT43 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.75985709G= , CM000676.2:g.75985709G= GRCh38
NC_000014.8:g.76452052G= , CM000676.1:g.76452052G= GRCh37
NC_000014.7:g.75521805G= NCBI36
NG_011715.1:g.1041C= , LRG_399:g.1041C=
NG_031957.1:g.4957G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000555677.5:n.90-3176G=