ClinGen Allele Registry
Allele Registry
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Canonical Allele Identifier:
CA422484883
Gene:
Linked Data
dbSNP Id:
rs1665422947
gnomAD v4:
1-192800691-C-G
MyVariant Identifiers:
chr1:g.192769821C>G (hg19)
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000001.11:g.192800691C>G , CM000663.2:g.192800691C>G
GRCh38
NC_000001.10:g.192769821C>G , CM000663.1:g.192769821C>G
GRCh37
NC_000001.9:g.191036444C>G
NCBI36
Transcript Alleles
HGVS
Amino-acid Change
ENST00000429211.2:n.121C>G
Search 100 bp 5'
Search 100 bp 3'