Canonical Allele Identifier: CA136960980
Gene:
MyVariant.info:
GRCh38 chr6:g.32604474T>C
GRCh37 chr6:g.32572251T>C
gnomAD v3:
6:32604474 T / C
gnomAD v4:
chr6-32604474-T-C
Joint Max Group AF 0.15832087 (SAS)
Genomes Max Group AF 0.15832087 (SAS)
dbSNP:
2858870
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.32604474T>C , CM000668.2:g.32604474T>C GRCh38
NC_000006.11:g.32572251T>C , CM000668.1:g.32572251T>C GRCh37
NC_000006.10:g.32680229T>C NCBI36
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