Canonical Allele Identifier: CA1060389862
Gene: LINC02357 HGNC NCBI

Linked Data

dbSNP Id: rs1714638961
gnomAD v3: 4-26083958-G-C
gnomAD v4: 4-26083958-G-C

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.26083958G>C , CM000666.2:g.26083958G>C GRCh38
NC_000004.11:g.26085580G>C , CM000666.1:g.26085580G>C GRCh37
NC_000004.10:g.25694678G>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_925506.1:n.1401+3368G>C
XR_925506.3:n.1408+3368G>C