ClinGen Allele Registry
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Canonical Allele Identifier:
CA12672239
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr7:g.50405553A>G
GRCh37
chr7:g.50473251A>G
Linked Data - Sequence & Population
gnomAD v2:
7:50473251 A / G
gnomAD v3:
7:50405553 A / G
gnomAD v4:
chr7-50405553-A-G
Joint Max Group AF
0.25948109 (NFE)
Genomes Max Group AF
0.25948109 (NFE)
Linked Data - NCBI & NCI
dbSNP:
6964969
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000007.14:g.50405553A>G , CM000669.2:g.50405553A>G
GRCh38
NC_000007.13:g.50473251A>G , CM000669.1:g.50473251A>G
GRCh37
NC_000007.12:g.50440745A>G
NCBI36
NG_034231.1:g.106471A>G
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