Canonical Allele Identifier: CA188383123
Gene:
MyVariant.info:
GRCh38 chr9:g.4981602C>T
GRCh37 chr9:g.4981602C>T
gnomAD v3:
9:4981602 C / T
gnomAD v4:
chr9-4981602-C-T
Joint Max Group AF 0.00040913 (SAS)
Genomes Max Group AF 0.00040913 (SAS)
dbSNP:
10758669
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.4981602C>T , CM000671.2:g.4981602C>T GRCh38
NC_000009.11:g.4981602C>T , CM000671.1:g.4981602C>T GRCh37
NC_000009.10:g.4971602C>T NCBI36
NG_009904.1:g.1358C>T , LRG_612:g.1358C>T
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