Canonical Allele Identifier: CA11826504
Gene: LINC02357 HGNC NCBI

Linked Data

dbSNP Id: rs10517086
gnomAD v2: 4-26085511-G-A
gnomAD v3: 4-26083889-G-A
gnomAD v4: 4-26083889-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.26083889G>A , CM000666.2:g.26083889G>A GRCh38
NC_000004.11:g.26085511G>A , CM000666.1:g.26085511G>A GRCh37
NC_000004.10:g.25694609G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_925506.1:n.1401+3299G>A
XR_925506.3:n.1408+3299G>A