Canonical Allele Identifier: CA1122483562
Gene:

Linked Data

dbSNP Id: rs1819675892

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.25551365_25551367del , CM000671.2:g.25551365_25551367del GRCh38
NC_000009.11:g.25551363_25551365del , CM000671.1:g.25551363_25551365del GRCh37
NC_000009.10:g.25541363_25541365del NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_929525.1:n.50-793_50-791del
XR_929525.2:n.674-793_674-791del