ClinGen Allele Registry
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Canonical Allele Identifier:
CA13727547
Gene:
Linked Data - Predicted Effect Evidence
MyVariant.info:
GRCh38
chr12:g.91113176T>G
GRCh37
chr12:g.91506953T>G
Linked Data - Sequence & Population
gnomAD v2:
12:91506953 T / G
gnomAD v3:
12:91113176 T / G
gnomAD v4:
chr12-91113176-T-G
Joint Max Group AF
0.86282292 (NFE)
Genomes Max Group AF
0.86282292 (NFE)
Linked Data - NCBI & NCI
dbSNP:
3759222
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000012.12:g.91113176T>G , CM000674.2:g.91113176T>G
GRCh38
NC_000012.11:g.91506953T>G , CM000674.1:g.91506953T>G
GRCh37
NC_000012.10:g.90031084T>G
NCBI36
Search 100 bp 5'
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