ClinGen Allele Registry
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Canonical Allele Identifier:
CA14325755
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr16:g.23601679A>G
GRCh37
chr16:g.23613000A>G
Linked Data - Sequence & Population
gnomAD v2:
16:23613000 A / G
gnomAD v3:
16:23601679 A / G
gnomAD v4:
chr16-23601679-A-G
Joint Max Group AF
0.30163089 (AFR)
Genomes Max Group AF
0.30163089 (AFR)
Linked Data - NCBI & NCI
dbSNP:
3096145
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000016.10:g.23601679A>G , CM000678.2:g.23601679A>G
GRCh38
NC_000016.9:g.23613000A>G , CM000678.1:g.23613000A>G
GRCh37
NC_000016.8:g.23520501A>G
NCBI36
NG_007406.1:g.44679T>C , LRG_308:g.44679T>C
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