ClinGen Allele Registry
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Canonical Allele Identifier:
CA37675604
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr1:g.218532385C>T
GRCh37
chr1:g.218705727C>T
Linked Data - Sequence & Population
gnomAD v2:
1:218705727 C / T
gnomAD v3:
1:218532385 C / T
gnomAD v4:
chr1-218532385-C-T
Linked Data - NCBI & NCI
dbSNP:
1023089003
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000001.11:g.218532385C>T , CM000663.2:g.218532385C>T
GRCh38
NC_000001.10:g.218705727C>T , CM000663.1:g.218705727C>T
GRCh37
NC_000001.9:g.216772350C>T
NCBI36
Search 100 bp 5'
Search 100 bp 3'