Canonical Allele Identifier: CA1445661419
Gene: LINC02357 HGNC NCBI

Linked Data

dbSNP Id: rs1714640029

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.26084039A>G , CM000666.2:g.26084039A>G GRCh38
NC_000004.11:g.26085661A>G , CM000666.1:g.26085661A>G GRCh37
NC_000004.10:g.25694759A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_925506.1:n.1401+3449A>G
XR_925506.3:n.1408+3449A>G