Canonical Allele Identifier: CA94354160
Gene: LINC02357 HGNC NCBI

Linked Data

dbSNP Id: rs760641934
gnomAD v3: 4-26083854-A-G
gnomAD v4: 4-26083854-A-G

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.26083854A>G , CM000666.2:g.26083854A>G GRCh38
NC_000004.11:g.26085476A>G , CM000666.1:g.26085476A>G GRCh37
NC_000004.10:g.25694574A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_925506.1:n.1401+3264A>G
XR_925506.3:n.1408+3264A>G