ClinGen Allele Registry
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Canonical Allele Identifier:
CA12188859
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr6:g.33010438G>A
GRCh37
chr6:g.32978215G>A
Linked Data - Sequence & Population
gnomAD v2:
6:32978215 G / A
gnomAD v3:
6:33010438 G / A
gnomAD v4:
chr6-33010438-G-A
Joint Max Group AF
0.32898105 (SAS)
Genomes Max Group AF
0.32898105 (SAS)
Linked Data - NCBI & NCI
dbSNP:
9276982
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000006.12:g.33010438G>A , CM000668.2:g.33010438G>A
GRCh38
NC_000006.11:g.32978215G>A , CM000668.1:g.32978215G>A
GRCh37
NC_000006.10:g.33086193G>A
NCBI36
NG_012007.1:g.4175C>T
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