Canonical Allele Identifier: CA337456882
Gene: LINC00278 HGNC NCBI

Linked Data

dbSNP Id: rs111639580
gnomAD v3: Y-3010711-C-T
gnomAD v4: Y-3010711-C-T

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.3010711C>T , CM000686.2:g.3010711C>T GRCh38
NC_000024.9:g.2878752C>T , CM000686.1:g.2878752C>T GRCh37
NC_000024.8:g.2938752C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_046502.1:n.222+7494C>T