ClinGen Allele Registry
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Canonical Allele Identifier:
CA11829972
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr4:g.61100555T>C
GRCh37
chr4:g.61966273T>C
Linked Data - Sequence & Population
gnomAD v2:
4:61966273 T / C
gnomAD v3:
4:61100555 T / C
gnomAD v4:
chr4-61100555-T-C
Joint Max Group AF
0.78696566 (AMR)
Genomes Max Group AF
0.78696566 (AMR)
Linked Data - NCBI & NCI
dbSNP:
4599440
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000004.12:g.61100555T>C , CM000666.2:g.61100555T>C
GRCh38
NC_000004.11:g.61966273T>C , CM000666.1:g.61966273T>C
GRCh37
NC_000004.10:g.61648868T>C
NCBI36
Search 100 bp 5'
Search 100 bp 3'