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Canonical Allele Identifier:
CA35069269
Gene:
Linked Data
dbSNP Id:
rs182788550
gnomAD v3:
1-192800676-C-A
gnomAD v4:
1-192800676-C-A
MyVariant Identifiers:
chr1:g.192769806C>A (hg19)
chr1:g.192800676C>A (hg38)
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000001.11:g.192800676C>A , CM000663.2:g.192800676C>A
GRCh38
NC_000001.10:g.192769806C>A , CM000663.1:g.192769806C>A
GRCh37
NC_000001.9:g.191036429C>A
NCBI36
Transcript Alleles
HGVS
Amino-acid Change
ENST00000429211.2:n.106C>A
Search 100 bp 5'
Search 100 bp 3'