ClinGen Allele Registry
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Canonical Allele Identifier:
CA15082327
Gene:
Linked Data - Predicted Effect Evidence
MyVariant.info:
GRCh38
chr1:g.157705207G>T
GRCh37
chr1:g.157674997G>T
Linked Data - Sequence & Population
gnomAD v2:
1:157674997 G / T
gnomAD v3:
1:157705207 G / T
gnomAD v4:
chr1-157705207-G-T
Joint Max Group AF
0.86450481 (AFR)
Genomes Max Group AF
0.86450481 (AFR)
Linked Data - NCBI & NCI
dbSNP:
2317230
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000001.11:g.157705207G>T , CM000663.2:g.157705207G>T
GRCh38
NC_000001.10:g.157674997G>T , CM000663.1:g.157674997G>T
GRCh37
NC_000001.9:g.155941621G>T
NCBI36
NG_023241.1:g.651C>A
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