ClinGen Allele Registry
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Canonical Allele Identifier:
CA101676616
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr4:g.99353076G>A
GRCh37
chr4:g.100274233G>A
Linked Data - Sequence & Population
gnomAD v3:
4:99353076 G / A
gnomAD v4:
chr4-99353076-G-A
Linked Data - NCBI & NCI
dbSNP:
1040613293
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000004.12:g.99353076G>A , CM000666.2:g.99353076G>A
GRCh38
NC_000004.11:g.100274233G>A , CM000666.1:g.100274233G>A
GRCh37
NC_000004.10:g.100493256G>A
NCBI36
NG_011718.1:g.4685C>T
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