ClinGen Allele Registry
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Canonical Allele Identifier:
CA165519166
Gene:
Linked Data - Predicted Effect Evidence
MyVariant.info:
GRCh38
chr7:g.117963766G>A
GRCh37
chr7:g.117603820G>A
Linked Data - Sequence & Population
gnomAD v2:
7:117603820 G / A
gnomAD v3:
7:117963766 G / A
gnomAD v4:
chr7-117963766-G-A
Linked Data - NCBI & NCI
dbSNP:
1013278
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000007.14:g.117963766G>A , CM000669.2:g.117963766G>A
GRCh38
NC_000007.13:g.117603820G>A , CM000669.1:g.117603820G>A
GRCh37
NC_000007.12:g.117391056G>A
NCBI36
Search 100 bp 5'
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