Canonical Allele Identifier: CA172383991
Gene: LINC00208 HGNC NCBI

Linked Data

dbSNP Id: rs1023480200
gnomAD v3: 8-11578052-G-A
gnomAD v4: 8-11578052-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.11578052G>A , CM000670.2:g.11578052G>A GRCh38
NC_000008.10:g.11435561G>A , CM000670.1:g.11435561G>A GRCh37
NC_000008.9:g.11472970G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_040035.1:n.784-318G>A