ClinGen Allele Registry
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Canonical Allele Identifier:
CA200491739
Gene:
Linked Data
dbSNP Id:
rs573378130
gnomAD v2:
9-132339185-T-C
gnomAD v3:
9-129576906-T-C
gnomAD v4:
9-129576906-T-C
MyVariant Identifiers:
chr9:g.132339185T>C (hg19)
chr9:g.129576906T>C (hg38)
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000009.12:g.129576906T>C , CM000671.2:g.129576906T>C
GRCh38
NC_000009.11:g.132339185T>C , CM000671.1:g.132339185T>C
GRCh37
NC_000009.10:g.131379006T>C
NCBI36
Transcript Alleles
HGVS
Amino-acid Change
XR_930390.1:n.182+1308T>C
Search 100 bp 5'
Search 100 bp 3'