Canonical Allele Identifier: CA2298481299
Gene:

Linked Data

dbSNP Id: rs1910120205
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Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.41477803del , CM000680.2:g.41477803del GRCh38
NC_000018.9:g.39057767del , CM000680.1:g.39057767del GRCh37
NC_000018.8:g.37311765del NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_935409.1:n.86-26331del
Search 100 bp 5'
Search 100 bp 3'