ClinGen Allele Registry
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Canonical Allele Identifier:
CA166741662
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr7:g.128239891A>C
GRCh37
chr7:g.127879944A>C
Linked Data - Sequence & Population
gnomAD v2:
7:127879944 A / C
gnomAD v3:
7:128239891 A / C
gnomAD v4:
chr7-128239891-A-C
Linked Data - NCBI & NCI
dbSNP:
13228377
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000007.14:g.128239891A>C , CM000669.2:g.128239891A>C
GRCh38
NC_000007.13:g.127879944A>C , CM000669.1:g.127879944A>C
GRCh37
NC_000007.12:g.127667180A>C
NCBI36
NG_007450.1:g.3614A>C
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