ClinGen Allele Registry
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Canonical Allele Identifier:
CA669931362
Gene: HECTD2-AS1
HGNC
NCBI
Linked Data
dbSNP Id:
rs1277425130
gnomAD v3:
10-91588396-A-T
gnomAD v4:
10-91588396-A-T
MyVariant Identifiers:
chr10:g.93348153A>T (hg19)
chr10:g.91588396A>T (hg38)
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000010.11:g.91588396A>T , CM000672.2:g.91588396A>T
GRCh38
NC_000010.10:g.93348153A>T , CM000672.1:g.93348153A>T
GRCh37
NC_000010.9:g.93338133A>T
NCBI36
Transcript Alleles
HGVS
Amino-acid Change
NR_024467.1:n.110+22955T>A
Search 100 bp 5'
Search 100 bp 3'