ClinGen Allele Registry
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Canonical Allele Identifier:
CA10912383
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr1:g.203187994G>A
GRCh37
chr1:g.203157122G>A
Linked Data - Sequence & Population
gnomAD v2:
1:203157122 G / A
gnomAD v3:
1:203187994 G / A
gnomAD v4:
chr1-203187994-G-A
Joint Max Group AF
0.29216176 (AMR)
Genomes Max Group AF
0.29216176 (AMR)
Linked Data - NCBI & NCI
dbSNP:
6691378
2100230530
2100230536
2100230547
2100230567
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000001.11:g.203187994G>A , CM000663.2:g.203187994G>A
GRCh38
NC_000001.10:g.203157122G>A , CM000663.1:g.203157122G>A
GRCh37
NC_000001.9:g.201423745G>A
NCBI36
NG_013056.1:g.3801C>T
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