ClinGen Allele Registry
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Canonical Allele Identifier:
CA203314755
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr10:g.18134451T>G
GRCh37
chr10:g.18423380T>G
Linked Data - Sequence & Population
gnomAD v3:
10:18134451 T / G
gnomAD v4:
chr10-18134451-T-G
Linked Data - NCBI & NCI
dbSNP:
2357790
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000010.11:g.18134451T>G , CM000672.2:g.18134451T>G
GRCh38
NC_000010.10:g.18423380T>G , CM000672.1:g.18423380T>G
GRCh37
NC_000010.9:g.18463386T>G
NCBI36
Search 100 bp 5'
Search 100 bp 3'