ClinGen Allele Registry
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Canonical Allele Identifier:
CA10991269
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr1:g.193765770G>A
GRCh37
chr1:g.193734900G>A
Linked Data - Sequence & Population
gnomAD v2:
1:193734900 G / A
gnomAD v3:
1:193765770 G / A
gnomAD v4:
chr1-193765770-G-A
Joint Max Group AF
0.05006935 (NFE)
Genomes Max Group AF
0.05006935 (NFE)
Linked Data - NCBI & NCI
dbSNP:
2025934
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000001.11:g.193765770G>A , CM000663.2:g.193765770G>A
GRCh38
NC_000001.10:g.193734900G>A , CM000663.1:g.193734900G>A
GRCh37
NC_000001.9:g.192001523G>A
NCBI36
Search 100 bp 5'
Search 100 bp 3'