Canonical Allele Identifier: CA965992684
Gene:

Linked Data

dbSNP Id: rs1884565958

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.92307359_92307361del , CM000676.2:g.92307359_92307361del GRCh38
NC_000014.8:g.92773703_92773705del , CM000676.1:g.92773703_92773705del GRCh37
NC_000014.7:g.91843456_91843458del NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_944153.1:n.131+2815_131+2817del