ClinGen Allele Registry
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Canonical Allele Identifier:
CA891212726
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr1:g.17307077G>A
GRCh37
chr1:g.17633572G>A
Linked Data - Sequence & Population
gnomAD v3:
1:17307077 G / A
gnomAD v4:
chr1-17307077-G-A
Linked Data - NCBI & NCI
dbSNP:
2477134
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000001.11:g.17307077G>A , CM000663.2:g.17307077G>A
GRCh38
NC_000001.10:g.17633572G>A , CM000663.1:g.17633572G>A
GRCh37
NC_000001.9:g.17506159G>A
NCBI36
Search 100 bp 5'
Search 100 bp 3'