ClinGen Allele Registry
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Canonical Allele Identifier:
CA307703719
Gene: HPN-AS1
HGNC
NCBI
Linked Data
dbSNP Id:
rs757676617
gnomAD v2:
19-35559426-G-A
gnomAD v3:
19-35068522-G-A
gnomAD v4:
19-35068522-G-A
MyVariant Identifiers:
chr19:g.35559426G>A (hg19)
chr19:g.35068522G>A (hg38)
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000019.10:g.35068522G>A , CM000681.2:g.35068522G>A
GRCh38
NC_000019.9:g.35559426G>A , CM000681.1:g.35559426G>A
GRCh37
NC_000019.8:g.40251266G>A
NCBI36
Transcript Alleles
HGVS
Amino-acid change
NR_024562.1:n.405-8744C>T
Search 100 bp 5'
Search 100 bp 3'