ClinGen Allele Registry
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Canonical Allele Identifier:
CA12077353
Gene:
Linked Data - Predicted Effect Evidence
MyVariant.info:
GRCh38
chr5:g.1450329C>T
GRCh37
chr5:g.1450444C>T
Linked Data - Sequence & Population
gnomAD v2:
5:1450444 C / T
gnomAD v3:
5:1450329 C / T
gnomAD v4:
chr5-1450329-C-T
Joint Max Group AF
0.58650346 (NFE)
Genomes Max Group AF
0.58650346 (NFE)
Linked Data - NCBI & NCI
dbSNP:
2550948
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000005.10:g.1450329C>T , CM000667.2:g.1450329C>T
GRCh38
NC_000005.9:g.1450444C>T , CM000667.1:g.1450444C>T
GRCh37
NC_000005.8:g.1503444C>T
NCBI36
NG_015885.1:g.100G>A
Search 100 bp 5'
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