ClinGen Allele Registry
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Canonical Allele Identifier:
CA600137043
Gene:
Linked Data - Predicted Effect Evidence
MyVariant.info:
GRCh38
chr11:g.69424973G>C
GRCh37
chr11:g.69239741G>C
Linked Data - Sequence & Population
gnomAD v2:
11:69239741 G / C
gnomAD v3:
11:69424973 G / C
gnomAD v4:
chr11-69424973-G-C
Linked Data - NCBI & NCI
dbSNP:
7105934
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000011.10:g.69424973G>C , CM000673.2:g.69424973G>C
GRCh38
NC_000011.9:g.69239741G>C , CM000673.1:g.69239741G>C
GRCh37
NC_000011.8:g.68948922G>C
NCBI36
Search 100 bp 5'
Search 100 bp 3'