ClinGen Allele Registry
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Canonical Allele Identifier:
CA15238308
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr3:g.148697390T>C
GRCh37
chr3:g.148415177T>C
Linked Data - Sequence & Population
gnomAD v2:
3:148415177 T / C
gnomAD v3:
3:148697390 T / C
gnomAD v4:
chr3-148697390-T-C
Joint Max Group AF
0.79187 (EAS)
Genomes Max Group AF
0.79187 (EAS)
Linked Data - NCBI & NCI
dbSNP:
1492078
2125141013
2125141016
2125141020
2125141033
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000003.12:g.148697390T>C , CM000665.2:g.148697390T>C
GRCh38
NC_000003.11:g.148415177T>C , CM000665.1:g.148415177T>C
GRCh37
NC_000003.10:g.149897867T>C
NCBI36
NG_008468.1:g.4520T>C
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