ClinGen Allele Registry
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Canonical Allele Identifier:
CA212023293
Gene: HECTD2-AS1
HGNC
NCBI
Linked Data
dbSNP Id:
rs997416902
gnomAD v3:
10-91590064-C-A
gnomAD v4:
10-91590064-C-A
MyVariant Identifiers:
chr10:g.93349821C>A (hg19)
chr10:g.91590064C>A (hg38)
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000010.11:g.91590064C>A , CM000672.2:g.91590064C>A
GRCh38
NC_000010.10:g.93349821C>A , CM000672.1:g.93349821C>A
GRCh37
NC_000010.9:g.93339801C>A
NCBI36
Transcript Alleles
HGVS
Amino-acid change
NR_024467.1:n.110+21287G>T
Search 100 bp 5'
Search 100 bp 3'