ClinGen Allele Registry
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Canonical Allele Identifier:
CA10988520
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr1:g.145711327T>G
GRCh37
chr1:g.145723739A>C
Linked Data - Sequence & Population
gnomAD v2:
1:145723739 A / C
gnomAD v3:
1:145711327 T / G
gnomAD v4:
chr1-145711327-T-G
Joint Max Group AF
0.52202885 (NFE)
Genomes Max Group AF
0.52202885 (NFE)
Linked Data - NCBI & NCI
dbSNP:
1471633
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000001.11:g.145711327T>G , CM000663.2:g.145711327T>G
GRCh38
NC_000001.10:g.145723739A>C , CM000663.1:g.145723739A>C
GRCh37
NC_000001.9:g.144435096A>C
NCBI36
NG_050630.1:g.1074A>C
NG_050630.2:g.1875A>C
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