ClinGen Allele Registry
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Canonical Allele Identifier:
CA786417412
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr4:g.122759930C>T
GRCh37
chr4:g.123681085C>T
Linked Data - Sequence & Population
gnomAD v3:
4:122759930 C / T
gnomAD v4:
chr4-122759930-C-T
Linked Data - NCBI & NCI
dbSNP:
1242153853
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000004.12:g.122759930C>T , CM000666.2:g.122759930C>T
GRCh38
NC_000004.11:g.123681085C>T , CM000666.1:g.123681085C>T
GRCh37
NC_000004.10:g.123900535C>T
NCBI36
Search 100 bp 5'
Search 100 bp 3'