ClinGen Allele Registry
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Canonical Allele Identifier:
CA14662614
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr19:g.44905371T>C
GRCh37
chr19:g.45408628T>C
Linked Data - Sequence & Population
gnomAD v2:
19:45408628 T / C
gnomAD v3:
19:44905371 T / C
gnomAD v4:
chr19-44905371-T-C
Joint Max Group AF
0.09702934 (NFE)
Genomes Max Group AF
0.09702934 (NFE)
Linked Data - NCBI & NCI
dbSNP:
769446
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000019.10:g.44905371T>C , CM000681.2:g.44905371T>C
GRCh38
NC_000019.9:g.45408628T>C , CM000681.1:g.45408628T>C
GRCh37
NC_000019.8:g.50100468T>C
NCBI36
NG_007084.2:g.4590T>C
NG_042854.1:g.19152T>C
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