ClinGen Allele Registry
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Canonical Allele Identifier:
CA10794576
Gene:
Linked Data - Predicted Effect Evidence
MyVariant.info:
GRCh38
chr1:g.239233804C>T
GRCh37
chr1:g.239397104C>T
Linked Data - Sequence & Population
gnomAD v2:
1:239397104 C / T
gnomAD v3:
1:239233804 C / T
gnomAD v4:
chr1-239233804-C-T
Joint Max Group AF
0.97415838 (AFR)
Genomes Max Group AF
0.97415838 (AFR)
Linked Data - NCBI & NCI
dbSNP:
1339738
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000001.11:g.239233804C>T , CM000663.2:g.239233804C>T
GRCh38
NC_000001.10:g.239397104C>T , CM000663.1:g.239397104C>T
GRCh37
NC_000001.9:g.237463727C>T
NCBI36
Search 100 bp 5'
Search 100 bp 3'