ClinGen Allele Registry
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Canonical Allele Identifier:
CA130189212
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr5:g.157603141del
GRCh37
chr5:g.157030149del
Linked Data - Sequence & Population
gnomAD v2:
5:157030148 TA / T
gnomAD v3:
5:157603140 TA / T
gnomAD v4:
chr5-157603140-TA-T
Joint Max Group AF
0.00004751 (AFR)
Genomes Max Group AF
0.00004751 (AFR)
Linked Data - NCBI & NCI
dbSNP:
891250397
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000005.10:g.157603148del , CM000667.2:g.157603148del
GRCh38
NC_000005.9:g.157030156del , CM000667.1:g.157030156del
GRCh37
NC_000005.8:g.156962734del
NCBI36
Search 100 bp 5'
Search 100 bp 3'