Canonical Allele Identifier: CA15393547
Gene: LINC02196 HGNC NCBI
MyVariant.info:
GRCh38 chr5:g.7096387G>A
GRCh37 chr5:g.7096500G>A
gnomAD v2:
5:7096500 G / A
gnomAD v3:
5:7096387 G / A
gnomAD v4:
chr5-7096387-G-A
Joint Max Group AF 0.38146305 (EAS)
Genomes Max Group AF 0.38146305 (EAS)
dbSNP:
7702920
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.7096387G>A , CM000667.2:g.7096387G>A GRCh38
NC_000005.9:g.7096500G>A , CM000667.1:g.7096500G>A GRCh37
NC_000005.8:g.7149500G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_001742592.1:n.86-52381G>A
Search 100 bp 5'
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