ClinGen Allele Registry
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Canonical Allele Identifier:
CA861673986
Gene:
Linked Data
dbSNP Id:
rs1157385624
MyVariant Identifiers:
chr9:g.1787380A>G (hg19)
chr9:g.1787380A>G (hg38)
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000009.12:g.1787380A>G , CM000671.2:g.1787380A>G
GRCh38
NC_000009.11:g.1787380A>G , CM000671.1:g.1787380A>G
GRCh37
NC_000009.10:g.1777380A>G
NCBI36
Transcript Alleles
HGVS
Amino-acid Change
XR_001746599.1:n.142+68468A>G
Search 100 bp 5'
Search 100 bp 3'