ClinGen Allele Registry
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Canonical Allele Identifier:
CA238787661
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr12:g.63154950G>A
GRCh37
chr12:g.63548730G>A
Linked Data - Sequence & Population
gnomAD v2:
12:63548730 G / A
gnomAD v3:
12:63154950 G / A
gnomAD v4:
chr12-63154950-G-A
Joint Max Group AF
0.02406641 (AFR)
Genomes Max Group AF
0.02406641 (AFR)
Linked Data - NCBI & NCI
dbSNP:
115757261
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000012.12:g.63154950G>A , CM000674.2:g.63154950G>A
GRCh38
NC_000012.11:g.63548730G>A , CM000674.1:g.63548730G>A
GRCh37
NC_000012.10:g.61834997G>A
NCBI36
Search 100 bp 5'
Search 100 bp 3'