ClinGen Allele Registry
Allele Registry
Register
Login
Forgot Login?
Canonical Allele Identifier:
CA606891626
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr12:g.91770525C>A
GRCh37
chr12:g.92164302C>A
Linked Data - Sequence & Population
gnomAD v2:
12:92164302 C / A
gnomAD v3:
12:91770525 C / A
gnomAD v4:
chr12-91770525-C-A
Linked Data - NCBI & NCI
dbSNP:
10777332
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000012.12:g.91770525C>A , CM000674.2:g.91770525C>A
GRCh38
NC_000012.11:g.92164302C>A , CM000674.1:g.92164302C>A
GRCh37
NC_000012.10:g.90688433C>A
NCBI36
Search 100 bp 5'
Search 100 bp 3'