ClinGen Allele Registry
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Canonical Allele Identifier:
CA785343171
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr4:g.110793263T>C
GRCh37
chr4:g.111714419T>C
Linked Data - Sequence & Population
gnomAD v3:
4:110793263 T / C
gnomAD v4:
chr4-110793263-T-C
Linked Data - NCBI & NCI
dbSNP:
13143308
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000004.12:g.110793263T>C , CM000666.2:g.110793263T>C
GRCh38
NC_000004.11:g.111714419T>C , CM000666.1:g.111714419T>C
GRCh37
NC_000004.10:g.111933868T>C
NCBI36
Search 100 bp 5'
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