ClinGen Allele Registry
Allele Registry
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Canonical Allele Identifier:
CA89976945
Gene:
Linked Data
dbSNP Id:
rs970116836
gnomAD v3:
3-187931538-C-T
gnomAD v4:
3-187931538-C-T
MyVariant Identifiers:
chr3:g.187649326C>T (hg19)
chr3:g.187931538C>T (hg38)
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000003.12:g.187931538C>T , CM000665.2:g.187931538C>T
GRCh38
NC_000003.11:g.187649326C>T , CM000665.1:g.187649326C>T
GRCh37
NC_000003.10:g.189132020C>T
NCBI36
Transcript Alleles
HGVS
Amino-acid Change
XR_924814.1:n.1376G>A
Search 100 bp 5'
Search 100 bp 3'