ClinGen Allele Registry
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Canonical Allele Identifier:
CA13265477
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr10:g.45373723T>C
GRCh37
chr10:g.45869171T>C
Linked Data - Sequence & Population
gnomAD v2:
10:45869171 T / C
gnomAD v3:
10:45373723 T / C
gnomAD v4:
chr10-45373723-T-C
Joint Max Group AF
0.17927947 (SAS)
Genomes Max Group AF
0.17927947 (SAS)
Linked Data - NCBI & NCI
dbSNP:
12762303
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000010.11:g.45373723T>C , CM000672.2:g.45373723T>C
GRCh38
NC_000010.10:g.45869171T>C , CM000672.1:g.45869171T>C
GRCh37
NC_000010.9:g.45189177T>C
NCBI36
NG_011437.1:g.4543T>C
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