ClinGen Allele Registry
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Canonical Allele Identifier:
CA136844219
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr6:g.31372298C>T
GRCh37
chr6:g.31340075C>T
Linked Data - Sequence & Population
gnomAD v2:
6:31340075 C / T
gnomAD v3:
6:31372298 C / T
gnomAD v4:
chr6-31372298-C-T
Joint Max Group AF
0.11852222 (NFE)
Genomes Max Group AF
0.11852222 (NFE)
Linked Data - NCBI & NCI
dbSNP:
2844559
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000006.12:g.31372298C>T , CM000668.2:g.31372298C>T
GRCh38
NC_000006.11:g.31340075C>T , CM000668.1:g.31340075C>T
GRCh37
NC_000006.10:g.31448054C>T
NCBI36
Search 100 bp 5'
Search 100 bp 3'