Canonical Allele Identifier: CA1842199339
Gene: C9orf72 HGNC NCBI

Linked Data

dbSNP Id: rs1820713238
gnomAD v4: 9-27543289-A-G

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.27543289A>G , CM000671.2:g.27543289A>G GRCh38
NC_000009.11:g.27543287A>G , CM000671.1:g.27543287A>G GRCh37
NC_000009.10:g.27533287A>G NCBI36
NG_031977.2:g.35578T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000673600.1:c.*267+4826T>C ENSP00000500650.1:n.*267+4826T>C
XR_001746639.2:n.856T>C