ClinGen Allele Registry
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Canonical Allele Identifier:
CA14686971
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr19:g.28998135T>A
GRCh37
chr19:g.29489042T>A
Linked Data - Sequence & Population
gnomAD v2:
19:29489042 T / A
gnomAD v3:
19:28998135 T / A
gnomAD v4:
chr19-28998135-T-A
Joint Max Group AF
0.6168115 (SAS)
Genomes Max Group AF
0.6168115 (SAS)
Linked Data - NCBI & NCI
dbSNP:
8102754
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000019.10:g.28998135T>A , CM000681.2:g.28998135T>A
GRCh38
NC_000019.9:g.29489042T>A , CM000681.1:g.29489042T>A
GRCh37
NC_000019.8:g.34180882T>A
NCBI36
Search 100 bp 5'
Search 100 bp 3'