ClinGen Allele Registry
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Canonical Allele Identifier:
CA307703721
Gene: HPN-AS1
HGNC
NCBI
Linked Data
dbSNP Id:
rs781720081
gnomAD v3:
19-35068532-A-C
gnomAD v4:
19-35068532-A-C
MyVariant Identifiers:
chr19:g.35559436A>C (hg19)
chr19:g.35068532A>C (hg38)
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000019.10:g.35068532A>C , CM000681.2:g.35068532A>C
GRCh38
NC_000019.9:g.35559436A>C , CM000681.1:g.35559436A>C
GRCh37
NC_000019.8:g.40251276A>C
NCBI36
Transcript Alleles
HGVS
Amino-acid Change
NR_024562.1:n.405-8754T>G
Search 100 bp 5'
Search 100 bp 3'