ClinGen Allele Registry
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Canonical Allele Identifier:
CA15776590
Gene:
Linked Data - Predicted Effect Evidence
MyVariant.info:
GRCh38
chr13:g.30765768G>C
GRCh37
chr13:g.31339905G>C
Linked Data - Sequence & Population
gnomAD v2:
13:31339905 G / C
gnomAD v3:
13:30765768 G / C
gnomAD v4:
chr13-30765768-G-C
Joint Max Group AF
0.11880237 (SAS)
Genomes Max Group AF
0.11880237 (SAS)
Linked Data - NCBI & NCI
dbSNP:
17239025
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000013.11:g.30765768G>C , CM000675.2:g.30765768G>C
GRCh38
NC_000013.10:g.31339905G>C , CM000675.1:g.31339905G>C
GRCh37
NC_000013.9:g.30237905G>C
NCBI36
NG_011963.2:g.57291G>C
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