Canonical Allele Identifier: CA793384466

Gene: LINC02357

Linked Data

• dbSNP Id: rs1172489665
• MyVariant Identifiers: chr4:g.26085614G>C (hg19) ; chr4:g.26083992G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.26083992G>C , CM000666.2:g.26083992G>C	GRCh38
NC_000004.11:g.26085614G>C , CM000666.1:g.26085614G>C	GRCh37
NC_000004.10:g.25694712G>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_925506.1:n.1401+3402G>C
XR_925506.3:n.1408+3402G>C