ClinGen Allele Registry
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Canonical Allele Identifier:
CA15977421
Gene:
Linked Data - Predicted Effect Evidence
MyVariant.info:
GRCh38
chr20:g.45916409C>T
GRCh37
chr20:g.44545048C>T
Linked Data - Sequence & Population
gnomAD v2:
20:44545048 C / T
gnomAD v3:
20:45916409 C / T
gnomAD v4:
chr20-45916409-C-T
Joint Max Group AF
0.74227284 (NFE)
Genomes Max Group AF
0.74227284 (NFE)
Linked Data - NCBI & NCI
dbSNP:
4810479
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000020.11:g.45916409C>T , CM000682.2:g.45916409C>T
GRCh38
NC_000020.10:g.44545048C>T , CM000682.1:g.44545048C>T
GRCh37
NC_000020.9:g.43978455C>T
NCBI36
NG_012115.1:g.739G>A
NG_012115.2:g.739G>A
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