Canonical Allele Identifier: CA11994963
Gene: LINC02226 HGNC NCBI
MyVariant.info:
GRCh38 chr5:g.8440615G>A
GRCh37 chr5:g.8440728G>A
gnomAD v2:
5:8440728 G / A
gnomAD v3:
5:8440615 G / A
gnomAD v4:
chr5-8440615-G-A
Joint Max Group AF 0.54148725 (AFR)
Genomes Max Group AF 0.54148725 (AFR)
dbSNP:
6555545
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.8440615G>A , CM000667.2:g.8440615G>A GRCh38
NC_000005.9:g.8440728G>A , CM000667.1:g.8440728G>A GRCh37
NC_000005.8:g.8493728G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_039984.1:n.174+11608C>T
Search 100 bp 5'
Search 100 bp 3'