ClinGen Allele Registry
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Canonical Allele Identifier:
CA570772149
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr6:g.137681038C>A
GRCh37
chr6:g.138002175C>A
Linked Data - Sequence & Population
gnomAD v2:
6:138002175 C / A
gnomAD v3:
6:137681038 C / A
gnomAD v4:
chr6-137681038-C-A
Linked Data - NCBI & NCI
dbSNP:
6927172
2113433517
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000006.12:g.137681038C>A , CM000668.2:g.137681038C>A
GRCh38
NC_000006.11:g.138002175C>A , CM000668.1:g.138002175C>A
GRCh37
NC_000006.10:g.138043868C>A
NCBI36
Search 100 bp 5'
Search 100 bp 3'