Canonical Allele Identifier: CA12139620
Gene: LINC02236 HGNC NCBI
MyVariant.info:
GRCh38 chr5:g.6813824G>T
GRCh37 chr5:g.6813937G>T
gnomAD v2:
5:6813937 G / T
gnomAD v3:
5:6813824 G / T
gnomAD v4:
chr5-6813824-G-T
Joint Max Group AF 0.30678696 (SAS)
Genomes Max Group AF 0.30678696 (SAS)
dbSNP:
275456
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.6813824G>T , CM000667.2:g.6813824G>T GRCh38
NC_000005.9:g.6813937G>T , CM000667.1:g.6813937G>T GRCh37
NC_000005.8:g.6866937G>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_146281.1:n.467-12819G>T
Search 100 bp 5'
Search 100 bp 3'