Canonical Allele Identifier: CA172383983
Gene: LINC00208 HGNC NCBI

Linked Data

dbSNP Id: rs536044302
gnomAD v3: 8-11578028-C-T
gnomAD v4: 8-11578028-C-T

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.11578028C>T , CM000670.2:g.11578028C>T GRCh38
NC_000008.10:g.11435537C>T , CM000670.1:g.11435537C>T GRCh37
NC_000008.9:g.11472946C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_040035.1:n.784-342C>T