ClinGen Allele Registry
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Canonical Allele Identifier:
CA104086662
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr4:g.110812980T>A
GRCh37
chr4:g.111734136T>A
Linked Data - Sequence & Population
gnomAD v2:
4:111734136 T / A
gnomAD v3:
4:110812980 T / A
gnomAD v4:
chr4-110812980-T-A
Linked Data - NCBI & NCI
dbSNP:
3853444
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000004.12:g.110812980T>A , CM000666.2:g.110812980T>A
GRCh38
NC_000004.11:g.111734136T>A , CM000666.1:g.111734136T>A
GRCh37
NC_000004.10:g.111953585T>A
NCBI36
Search 100 bp 5'
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