Canonical Allele Identifier: CA12796648
Gene: LINC00536 HGNC NCBI
COSMIC:
COSN17600258 (not active)
MyVariant.info:
GRCh38 chr8:g.116197325A>G
GRCh37 chr8:g.117209548A>G
gnomAD v2:
8:117209548 A / G
gnomAD v3:
8:116197325 A / G
gnomAD v4:
chr8-116197325-A-G
Joint Max Group AF 0.63681529 (NFE)
Genomes Max Group AF 0.63681529 (NFE)
dbSNP:
13267382
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.116197325A>G , CM000670.2:g.116197325A>G GRCh38
NC_000008.10:g.117209548A>G , CM000670.1:g.117209548A>G GRCh37
NC_000008.9:g.117278729A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_046215.1:n.1333+62167T>C
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