ClinGen Allele Registry
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Canonical Allele Identifier:
CA11562138
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr3:g.179455191G>T
GRCh37
chr3:g.179172979G>T
Linked Data - Sequence & Population
gnomAD v2:
3:179172979 G / T
gnomAD v3:
3:179455191 G / T
gnomAD v4:
chr3-179455191-G-T
Joint Max Group AF
0.38037832 (MID)
Genomes Max Group AF
0.3525748 (AFR)
Linked Data - NCBI & NCI
dbSNP:
7612445
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000003.12:g.179455191G>T , CM000665.2:g.179455191G>T
GRCh38
NC_000003.11:g.179172979G>T , CM000665.1:g.179172979G>T
GRCh37
NC_000003.10:g.180655673G>T
NCBI36
NG_033163.1:g.1393C>A
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