ClinGen Allele Registry
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Canonical Allele Identifier:
CA188145889
Gene:
Linked Data
dbSNP Id:
rs11998763
gnomAD v2:
9-1787687-G-A
gnomAD v3:
9-1787687-G-A
gnomAD v4:
9-1787687-G-A
MyVariant Identifiers:
chr9:g.1787687G>A (hg19)
chr9:g.1787687G>A (hg38)
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000009.12:g.1787687G>A , CM000671.2:g.1787687G>A
GRCh38
NC_000009.11:g.1787687G>A , CM000671.1:g.1787687G>A
GRCh37
NC_000009.10:g.1777687G>A
NCBI36
Transcript Alleles
HGVS
Amino-acid change
XR_001746599.1:n.142+68775G>A
Search 100 bp 5'
Search 100 bp 3'