ClinGen Allele Registry
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Canonical Allele Identifier:
CA188145830
Gene:
Linked Data
dbSNP Id:
rs896824025
gnomAD v3:
9-1787367-G-A
gnomAD v4:
9-1787367-G-A
MyVariant Identifiers:
chr9:g.1787367G>A (hg19)
chr9:g.1787367G>A (hg38)
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000009.12:g.1787367G>A , CM000671.2:g.1787367G>A
GRCh38
NC_000009.11:g.1787367G>A , CM000671.1:g.1787367G>A
GRCh37
NC_000009.10:g.1777367G>A
NCBI36
Transcript Alleles
HGVS
Amino-acid Change
XR_001746599.1:n.142+68455G>A
Search 100 bp 5'
Search 100 bp 3'