ClinGen Allele Registry
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Canonical Allele Identifier:
CA13639153
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr12:g.131378358G>A
GRCh37
chr12:g.131862903G>A
Linked Data - Sequence & Population
gnomAD v2:
12:131862903 G / A
gnomAD v3:
12:131378358 G / A
gnomAD v4:
chr12-131378358-G-A
Joint Max Group AF
0.38144684 (AFR)
Genomes Max Group AF
0.38144684 (AFR)
Linked Data - NCBI & NCI
dbSNP:
7965445
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000012.12:g.131378358G>A , CM000674.2:g.131378358G>A
GRCh38
NC_000012.11:g.131862903G>A , CM000674.1:g.131862903G>A
GRCh37
NC_000012.10:g.130428856G>A
NCBI36
Search 100 bp 5'
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