Canonical Allele Identifier: CA15781200
Gene: LINC02343 HGNC NCBI
COSMIC:
COSN6623137 (not active)
MyVariant.info:
GRCh38 chr13:g.34376390C>T
GRCh37 chr13:g.34950527C>T
gnomAD v2:
13:34950527 C / T
gnomAD v3:
13:34376390 C / T
gnomAD v4:
chr13-34376390-C-T
Joint Max Group AF 0.19954237 (SAS)
Genomes Max Group AF 0.19954237 (SAS)
dbSNP:
17798800
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Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.34376390C>T , CM000675.2:g.34376390C>T GRCh38
NC_000013.10:g.34950527C>T , CM000675.1:g.34950527C>T GRCh37
NC_000013.9:g.33848527C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_941846.1:n.182+28266C>T
XR_941847.1:n.182+28266C>T
XR_941848.1:n.180+28266C>T
NR_146542.1:n.82+28266C>T
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