Canonical Allele Identifier: CA13329527
Gene:
COSMIC:
COSN17597602 (not active)
MyVariant.info:
GRCh38 chr10:g.8677306C>T
GRCh37 chr10:g.8719269C>T
gnomAD v2:
10:8719269 C / T
gnomAD v3:
10:8677306 C / T
gnomAD v4:
chr10-8677306-C-T
Joint Max Group AF 0.81182837 (AMR)
Genomes Max Group AF 0.81182837 (AMR)
dbSNP:
827382
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.8677306C>T , CM000672.2:g.8677306C>T GRCh38
NC_000010.10:g.8719269C>T , CM000672.1:g.8719269C>T GRCh37
NC_000010.9:g.8759275C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_930641.1:n.33-7505G>A
Search 100 bp 5'
Search 100 bp 3'