ClinGen Allele Registry
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Canonical Allele Identifier:
CA212296882
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr10:g.102837961G>A
GRCh37
chr10:g.104597718G>A
Linked Data - Sequence & Population
gnomAD v2:
10:104597718 G / A
gnomAD v3:
10:102837961 G / A
gnomAD v4:
chr10-102837961-G-A
Joint Max Group AF
0.0000173 (NFE)
Genomes Max Group AF
0.00001972 (NFE)
Linked Data - NCBI & NCI
dbSNP:
17115149
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000010.11:g.102837961G>A , CM000672.2:g.102837961G>A
GRCh38
NC_000010.10:g.104597718G>A , CM000672.1:g.104597718G>A
GRCh37
NC_000010.9:g.104587708G>A
NCBI36
NG_007955.1:g.4573C>T
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