Canonical Allele Identifier: CA202788802
Gene:

Linked Data

dbSNP Id: rs796768291
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.8697701_8697702delinsCG , CM000672.2:g.8697701_8697702delinsCG GRCh38
NC_000010.10:g.8739664_8739665delinsCG , CM000672.1:g.8739664_8739665delinsCG GRCh37
NC_000010.9:g.8779670_8779671delinsCG NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_930641.1:n.33-27901_33-27900delinsCG
Search 100 bp 5'
Search 100 bp 3'