ClinGen Allele Registry
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Canonical Allele Identifier:
CA548332332
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr3:g.169765072G>A
GRCh37
chr3:g.169482860G>A
Linked Data - Sequence & Population
gnomAD v2:
3:169482860 G / A
gnomAD v4:
chr3-169765072-G-A
Linked Data - NCBI & NCI
dbSNP:
761453569
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000003.12:g.169765072G>A , CM000665.2:g.169765072G>A
GRCh38
NC_000003.11:g.169482860G>A , CM000665.1:g.169482860G>A
GRCh37
NC_000003.10:g.170965554G>A
NCBI36
NG_016363.1:g.4989C>T , LRG_347:g.4989C>T
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