Canonical Allele Identifier: CA94354175

Gene: LINC02357

Linked Data

• dbSNP Id: rs914384594
• gnomAD v2: 4-26085575-CT-C
• gnomAD v3: 4-26083953-CT-C
• gnomAD v4: 4-26083953-CT-C
• MyVariant Identifiers: chr4:g.26085576del (hg19) ; chr4:g.26083954del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.26083955del , CM000666.2:g.26083955del	GRCh38
NC_000004.11:g.26085577del , CM000666.1:g.26085577del	GRCh37
NC_000004.10:g.25694675del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_925506.1:n.1401+3365del
XR_925506.3:n.1408+3365del