ClinGen Allele Registry
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Canonical Allele Identifier:
CA606998935
Gene:
Linked Data - Predicted Effect Evidence
MyVariant.info:
GRCh38
chr12:g.96044775G>C
GRCh37
chr12:g.96438553G>C
Linked Data - Sequence & Population
gnomAD v2:
12:96438553 G / C
gnomAD v3:
12:96044775 G / C
gnomAD v4:
chr12-96044775-G-C
Linked Data - NCBI & NCI
dbSNP:
2660845
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000012.12:g.96044775G>C , CM000674.2:g.96044775G>C
GRCh38
NC_000012.11:g.96438553G>C , CM000674.1:g.96438553G>C
GRCh37
NC_000012.10:g.94962684G>C
NCBI36
Search 100 bp 5'
Search 100 bp 3'