ClinGen Allele Registry
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Canonical Allele Identifier:
CA188145846
Gene:
Linked Data
dbSNP Id:
rs928368589
gnomAD v2:
9-1787446-T-C
gnomAD v3:
9-1787446-T-C
gnomAD v4:
9-1787446-T-C
MyVariant Identifiers:
chr9:g.1787446T>C (hg19)
chr9:g.1787446T>C (hg38)
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000009.12:g.1787446T>C , CM000671.2:g.1787446T>C
GRCh38
NC_000009.11:g.1787446T>C , CM000671.1:g.1787446T>C
GRCh37
NC_000009.10:g.1777446T>C
NCBI36
Transcript Alleles
HGVS
Amino-acid Change
XR_001746599.1:n.142+68534T>C
Search 100 bp 5'
Search 100 bp 3'