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Canonical Allele Identifier:
CA232748328
Gene: CLECL1P
HGNC
NCBI
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr12:g.9703362T>G
GRCh37
chr12:g.9855958T>G
Linked Data - Sequence & Population
gnomAD v2:
12:9855958 T / G
gnomAD v3:
12:9703362 T / G
gnomAD v4:
chr12-9703362-T-G
Joint Max Group AF
0.59841396 (EAS)
Genomes Max Group AF
0.59841396 (EAS)
Linked Data - NCBI & NCI
dbSNP:
11052552
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000012.12:g.9703362T>G , CM000674.2:g.9703362T>G
GRCh38
NC_000012.11:g.9855958T>G , CM000674.1:g.9855958T>G
GRCh37
NC_000012.10:g.9747225T>G
NCBI36
Transcript Alleles
HGVS
Amino-acid Change
ENST00000702603.1:n.320-922A>C
Search 100 bp 5'
Search 100 bp 3'