Canonical Allele Identifier: CA15137589
Gene:
COSMIC:
COSN24801354 (not active)
MyVariant.info:
GRCh38 chr1:g.172658358C>T
GRCh37 chr1:g.172627498C>T
gnomAD v2:
1:172627498 C / T
gnomAD v3:
1:172658358 C / T
gnomAD v4:
chr1-172658358-C-T
Joint Max Group AF 0.80232388 (AFR)
Genomes Max Group AF 0.80232388 (AFR)
ClinVar RCV:
RCV001511738
ClinVar Variation:
1165021
dbSNP:
763110
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.172658358C>T , CM000663.2:g.172658358C>T GRCh38
NC_000001.10:g.172627498C>T , CM000663.1:g.172627498C>T GRCh37
NC_000001.9:g.170894121C>T NCBI36
NG_007269.1:g.4314C>T , LRG_58:g.4314C>T
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