Canonical Allele Identifier: CA793390824
Gene: LINC02357 HGNC NCBI
MyVariant.info:
GRCh38 chr4:g.26097188G>T
GRCh37 chr4:g.26098810G>T
gnomAD v3:
4:26097188 G / T
gnomAD v4:
chr4-26097188-G-T
Joint Max Group AF 0.00000488 (NFE)
Genomes Max Group AF 0.00000488 (NFE)
dbSNP:
6448432
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.26097188G>T , CM000666.2:g.26097188G>T GRCh38
NC_000004.11:g.26098810G>T , CM000666.1:g.26098810G>T GRCh37
NC_000004.10:g.25707908G>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_925506.1:n.1402-6857G>T
XR_925506.3:n.1409-6857G>T
Search 100 bp 5'
Search 100 bp 3'