Canonical Allele Identifier: CA11436432
Gene:
MyVariant.info:
GRCh38 chr3:g.9748191T>C
GRCh37 chr3:g.9789875T>C
gnomAD v2:
3:9789875 T / C
gnomAD v3:
3:9748191 T / C
gnomAD v4:
chr3-9748191-T-C
Joint Max Group AF 0.35370834 (AFR)
Genomes Max Group AF 0.35370834 (AFR)
dbSNP:
159153
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.9748191T>C , CM000665.2:g.9748191T>C GRCh38
NC_000003.11:g.9789875T>C , CM000665.1:g.9789875T>C GRCh37
NC_000003.10:g.9764875T>C NCBI36
NG_012106.1:g.3248T>C
NG_052955.1:g.21463T>C
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