ClinGen Allele Registry
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Canonical Allele Identifier:
CA612225678
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr13:g.105545931C>T
GRCh37
chr13:g.106198280C>T
Linked Data - Sequence & Population
gnomAD v2:
13:106198280 C / T
gnomAD v3:
13:105545931 C / T
gnomAD v4:
chr13-105545931-C-T
Linked Data - NCBI & NCI
dbSNP:
1488117878
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000013.11:g.105545931C>T , CM000675.2:g.105545931C>T
GRCh38
NC_000013.10:g.106198280C>T , CM000675.1:g.106198280C>T
GRCh37
NC_000013.9:g.104996281C>T
NCBI36
Search 100 bp 5'
Search 100 bp 3'