Canonical Allele Identifier: CA94354165

Gene: LINC02357

Linked Data

• dbSNP Id: rs186560308
• gnomAD v2: 4-26085491-T-C
• gnomAD v3: 4-26083869-T-C
• gnomAD v4: 4-26083869-T-C
• MyVariant Identifiers: chr4:g.26085491T>C (hg19) ; chr4:g.26083869T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.26083869T>C , CM000666.2:g.26083869T>C	GRCh38
NC_000004.11:g.26085491T>C , CM000666.1:g.26085491T>C	GRCh37
NC_000004.10:g.25694589T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_925506.1:n.1401+3279T>C
XR_925506.3:n.1408+3279T>C