ClinGen Allele Registry
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Canonical Allele Identifier:
CA693572586
Gene:
Linked Data
dbSNP Id:
rs1222482580
gnomAD v3:
12-93293316-C-A
gnomAD v4:
12-93293316-C-A
MyVariant Identifiers:
chr12:g.93687092C>A (hg19)
chr12:g.93293316C>A (hg38)
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000012.12:g.93293316C>A , CM000674.2:g.93293316C>A
GRCh38
NC_000012.11:g.93687092C>A , CM000674.1:g.93687092C>A
GRCh37
NC_000012.10:g.92211223C>A
NCBI36
Transcript Alleles
HGVS
Amino-acid Change
NR_040096.1:n.329+34711G>T
Search 100 bp 5'
Search 100 bp 3'