ClinGen Allele Registry
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Canonical Allele Identifier:
CA104889142
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr4:g.125510764C>T
GRCh37
chr4:g.126431919C>T
Linked Data - Sequence & Population
gnomAD v2:
4:126431919 C / T
gnomAD v3:
4:125510764 C / T
gnomAD v4:
chr4-125510764-C-T
Joint Max Group AF
0.86261615 (AFR)
Genomes Max Group AF
0.86261615 (AFR)
Linked Data - NCBI & NCI
dbSNP:
950063
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000004.12:g.125510764C>T , CM000666.2:g.125510764C>T
GRCh38
NC_000004.11:g.126431919C>T , CM000666.1:g.126431919C>T
GRCh37
NC_000004.10:g.126651369C>T
NCBI36
Search 100 bp 5'
Search 100 bp 3'