Canonical Allele Identifier: CA193640631
Gene:
MyVariant.info:
GRCh38 chr9:g.73543766G>T
GRCh37 chr9:g.76158682G>T
gnomAD v3:
9:73543766 G / T
gnomAD v4:
chr9-73543766-G-T
Joint Max Group AF 0.00001921 (AFR)
Genomes Max Group AF 0.00001921 (AFR)
dbSNP:
11143609
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.73543766G>T , CM000671.2:g.73543766G>T GRCh38
NC_000009.11:g.76158682G>T , CM000671.1:g.76158682G>T GRCh37
NC_000009.10:g.75348502G>T NCBI36
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