ClinGen Allele Registry
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Canonical Allele Identifier:
CA732527830
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr1:g.228862010G>T
GRCh37
chr1:g.228997757G>T
Linked Data - Sequence & Population
gnomAD v3:
1:228862010 G / T
gnomAD v4:
chr1-228862010-G-T
Linked Data - NCBI & NCI
dbSNP:
1340593499
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000001.11:g.228862010G>T , CM000663.2:g.228862010G>T
GRCh38
NC_000001.10:g.228997757G>T , CM000663.1:g.228997757G>T
GRCh37
NC_000001.9:g.227064380G>T
NCBI36
Search 100 bp 5'
Search 100 bp 3'