ClinGen Allele Registry
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Canonical Allele Identifier:
CA14634499
Gene:
Linked Data - Predicted Effect Evidence
MyVariant.info:
GRCh38
chr19:g.8579147G>C
GRCh37
chr19:g.8644031G>C
Linked Data - Sequence & Population
gnomAD v2:
19:8644031 G / C
gnomAD v3:
19:8579147 G / C
gnomAD v4:
chr19-8579147-G-C
Joint Max Group AF
0.73419807 (EAS)
Genomes Max Group AF
0.73419807 (EAS)
Linked Data - NCBI & NCI
dbSNP:
4072910
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000019.10:g.8579147G>C , CM000681.2:g.8579147G>C
GRCh38
NC_000019.9:g.8644031G>C , CM000681.1:g.8644031G>C
GRCh37
NC_000019.8:g.8550031G>C
NCBI36
NG_011840.2:g.36556C>G
NG_052844.1:g.3301C>G
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