Canonical Allele Identifier: CA172383990
Gene: LINC00208 HGNC NCBI

Linked Data

dbSNP Id: rs749859787
gnomAD v3: 8-11578051-C-T
gnomAD v4: 8-11578051-C-T

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.11578051C>T , CM000670.2:g.11578051C>T GRCh38
NC_000008.10:g.11435560C>T , CM000670.1:g.11435560C>T GRCh37
NC_000008.9:g.11472969C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_040035.1:n.784-319C>T