ClinGen Allele Registry
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Canonical Allele Identifier:
CA163327786
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr7:g.101126430A>G
GRCh37
chr7:g.100769711A>G
Linked Data - NCBI & NCI
dbSNP:
1799889
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000007.14:g.101126430A>G , CM000669.2:g.101126430A>G
GRCh38
NC_000007.13:g.100769711A>G , CM000669.1:g.100769711A>G
GRCh37
NC_000007.12:g.100556431A>G
NCBI36
NG_013213.1:g.4333A>G , LRG_597:g.4333A>G
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