Canonical Allele Identifier: CA1060389869
Gene: LINC02357 HGNC NCBI

Linked Data

dbSNP Id: rs1714639506
gnomAD v3: 4-26084007-G-T
gnomAD v4: 4-26084007-G-T

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.26084007G>T , CM000666.2:g.26084007G>T GRCh38
NC_000004.11:g.26085629G>T , CM000666.1:g.26085629G>T GRCh37
NC_000004.10:g.25694727G>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_925506.1:n.1401+3417G>T
XR_925506.3:n.1408+3417G>T