Canonical Allele Identifier: CA16260134
Gene:
MyVariant.info:
GRCh38 chr6:g.32608701T>C
GRCh37 chr6:g.32576478T>C
gnomAD v3:
6:32608701 T / C
gnomAD v4:
chr6-32608701-T-C
Joint Max Group AF 0.78347083 (EAS)
Genomes Max Group AF 0.78347083 (EAS)
dbSNP:
9271100
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.32608701T>C , CM000668.2:g.32608701T>C GRCh38
NC_000006.11:g.32576478T>C , CM000668.1:g.32576478T>C GRCh37
NC_000006.10:g.32684456T>C NCBI36
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