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Canonical Allele Identifier:
CA10902744
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr1:g.63661797C>G
GRCh37
chr1:g.64127468C>G
Linked Data - Sequence & Population
gnomAD v2:
1:64127468 C / G
gnomAD v3:
1:63661797 C / G
gnomAD v4:
chr1-63661797-C-G
Joint Max Group AF
0.28169477 (AMR)
Genomes Max Group AF
0.28169477 (AMR)
Linked Data - NCBI & NCI
dbSNP:
2749097
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000001.11:g.63661797C>G , CM000663.2:g.63661797C>G
GRCh38
NC_000001.10:g.64127468C>G , CM000663.1:g.64127468C>G
GRCh37
NC_000001.9:g.63900056C>G
NCBI36
NG_016966.1:g.73522C>G
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