ClinGen Allele Registry
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Canonical Allele Identifier:
CA28974652
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr1:g.113761230G>A
GRCh37
chr1:g.114303852G>A
Linked Data - Sequence & Population
gnomAD v3:
1:113761230 G / A
gnomAD v4:
chr1-113761230-G-A
Linked Data - NCBI & NCI
dbSNP:
893716164
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000001.11:g.113761230G>A , CM000663.2:g.113761230G>A
GRCh38
NC_000001.10:g.114303852G>A , CM000663.1:g.114303852G>A
GRCh37
NC_000001.9:g.114105375G>A
NCBI36
Search 100 bp 5'
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