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Canonical Allele Identifier:
CA15178583
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr2:g.25170385C>T
GRCh37
chr2:g.25393254C>T
Linked Data - Sequence & Population
gnomAD v2:
2:25393254 C / T
gnomAD v3:
2:25170385 C / T
gnomAD v4:
chr2-25170385-C-T
Joint Max Group AF
0.32085041 (SAS)
Genomes Max Group AF
0.32085041 (SAS)
Linked Data - NCBI & NCI
dbSNP:
3754860
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000002.12:g.25170385C>T , CM000664.2:g.25170385C>T
GRCh38
NC_000002.11:g.25393254C>T , CM000664.1:g.25393254C>T
GRCh37
NC_000002.10:g.25246758C>T
NCBI36
NG_008997.1:g.3306G>A
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