Canonical Allele Identifier: CA1060389868

Gene: LINC02357

Linked Data

• dbSNP Id: rs1714639435
• gnomAD v3: 4-26083998-T-C
• gnomAD v4: 4-26083998-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.26083998T>C , CM000666.2:g.26083998T>C	GRCh38
NC_000004.11:g.26085620T>C , CM000666.1:g.26085620T>C	GRCh37
NC_000004.10:g.25694718T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_925506.1:n.1401+3408T>C
XR_925506.3:n.1408+3408T>C