Canonical Allele Identifier: CA94354155
Gene: LINC02357 HGNC NCBI

Linked Data

dbSNP Id: rs556381195
gnomAD v3: 4-26083818-G-C
gnomAD v4: 4-26083818-G-C

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.26083818G>C , CM000666.2:g.26083818G>C GRCh38
NC_000004.11:g.26085440G>C , CM000666.1:g.26085440G>C GRCh37
NC_000004.10:g.25694538G>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_925506.1:n.1401+3228G>C
XR_925506.3:n.1408+3228G>C