ClinGen Allele Registry
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Canonical Allele Identifier:
CA238094444
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr12:g.60416871T>C
GRCh37
chr12:g.60810652T>C
Linked Data - Sequence & Population
gnomAD v2:
12:60810652 T / C
gnomAD v3:
12:60416871 T / C
gnomAD v4:
chr12-60416871-T-C
Joint Max Group AF
0.53941097 (AFR)
Genomes Max Group AF
0.53941097 (AFR)
Linked Data - NCBI & NCI
dbSNP:
2655898
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000012.12:g.60416871T>C , CM000674.2:g.60416871T>C
GRCh38
NC_000012.11:g.60810652T>C , CM000674.1:g.60810652T>C
GRCh37
NC_000012.10:g.59096919T>C
NCBI36
Search 100 bp 5'
Search 100 bp 3'