ClinGen Allele Registry
Allele Registry
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Canonical Allele Identifier:
CA241972489
Gene:
Linked Data
dbSNP Id:
rs527314861
gnomAD v3:
12-93293137-A-G
gnomAD v4:
12-93293137-A-G
MyVariant Identifiers:
chr12:g.93686913A>G (hg19)
chr12:g.93293137A>G (hg38)
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000012.12:g.93293137A>G , CM000674.2:g.93293137A>G
GRCh38
NC_000012.11:g.93686913A>G , CM000674.1:g.93686913A>G
GRCh37
NC_000012.10:g.92211044A>G
NCBI36
Transcript Alleles
HGVS
Amino-acid Change
NR_040096.1:n.329+34890T>C
Search 100 bp 5'
Search 100 bp 3'