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Canonical Allele Identifier:
CA13171157
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr10:g.119551536G>C
GRCh37
chr10:g.121311048G>C
Linked Data - Sequence & Population
gnomAD v2:
10:121311048 G / C
gnomAD v3:
10:119551536 G / C
gnomAD v4:
chr10-119551536-G-C
Joint Max Group AF
0.50162704 (EAS)
Genomes Max Group AF
0.50162704 (EAS)
Linked Data - NCBI & NCI
dbSNP:
10510057
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000010.11:g.119551536G>C , CM000672.2:g.119551536G>C
GRCh38
NC_000010.10:g.121311048G>C , CM000672.1:g.121311048G>C
GRCh37
NC_000010.9:g.121301038G>C
NCBI36
Search 100 bp 5'
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