ClinGen Allele Registry
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Canonical Allele Identifier:
CA11059367
Gene:
Linked Data - Predicted Effect Evidence
MyVariant.info:
GRCh38
chr2:g.19121042T>C
GRCh37
chr2:g.19320803T>C
Linked Data - Sequence & Population
gnomAD v2:
2:19320803 T / C
gnomAD v3:
2:19121042 T / C
gnomAD v4:
chr2-19121042-T-C
Joint Max Group AF
0.67796562 (EAS)
Genomes Max Group AF
0.67796562 (EAS)
Linked Data - NCBI & NCI
dbSNP:
12710696
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000002.12:g.19121042T>C , CM000664.2:g.19121042T>C
GRCh38
NC_000002.11:g.19320803T>C , CM000664.1:g.19320803T>C
GRCh37
NC_000002.10:g.19184284T>C
NCBI36
Search 100 bp 5'
Search 100 bp 3'