ClinGen Allele Registry
Allele Registry
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Canonical Allele Identifier:
CA860367887
Gene:
Linked Data
dbSNP Id:
rs1222062398
gnomAD v3:
9-129576829-G-A
gnomAD v4:
9-129576829-G-A
MyVariant Identifiers:
chr9:g.132339108G>A (hg19)
chr9:g.129576829G>A (hg38)
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000009.12:g.129576829G>A , CM000671.2:g.129576829G>A
GRCh38
NC_000009.11:g.132339108G>A , CM000671.1:g.132339108G>A
GRCh37
NC_000009.10:g.131378929G>A
NCBI36
Transcript Alleles
HGVS
Amino-acid Change
XR_930390.1:n.182+1231G>A
Search 100 bp 5'
Search 100 bp 3'