ClinGen Allele Registry
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Canonical Allele Identifier:
CA800725957
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr4:g.99353070A>G
GRCh37
chr4:g.100274227A>G
Linked Data - Sequence & Population
gnomAD v4:
chr4-99353070-A-G
Linked Data - NCBI & NCI
dbSNP:
1267255594
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000004.12:g.99353070A>G , CM000666.2:g.99353070A>G
GRCh38
NC_000004.11:g.100274227A>G , CM000666.1:g.100274227A>G
GRCh37
NC_000004.10:g.100493250A>G
NCBI36
NG_011718.1:g.4691T>C
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