ClinGen Allele Registry
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Canonical Allele Identifier:
CA669931498
Gene: HECTD2-AS1
HGNC
NCBI
Linked Data
dbSNP Id:
rs1161578384
MyVariant Identifiers:
chr10:g.93349716del (hg19)
chr10:g.91589959del (hg38)
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000010.11:g.91589959del , CM000672.2:g.91589959del
GRCh38
NC_000010.10:g.93349716del , CM000672.1:g.93349716del
GRCh37
NC_000010.9:g.93339696del
NCBI36
Transcript Alleles
HGVS
Amino-acid change
NR_024467.1:n.110+21392del
Search 100 bp 5'
Search 100 bp 3'