Canonical Allele Identifier: CA2705535590
Gene: LINC02357 HGNC NCBI

Linked Data

dbSNP Id: rs2109066090

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.26083829T>C , CM000666.2:g.26083829T>C GRCh38
NC_000004.11:g.26085451T>C , CM000666.1:g.26085451T>C GRCh37
NC_000004.10:g.25694549T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_925506.1:n.1401+3239T>C
XR_925506.3:n.1408+3239T>C