Canonical Allele Identifier: CA846003730
Gene: LINC00208 HGNC NCBI

Linked Data

dbSNP Id: rs1300367354
gnomAD v3: 8-11577977-A-G
gnomAD v4: 8-11577977-A-G

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.11577977A>G , CM000670.2:g.11577977A>G GRCh38
NC_000008.10:g.11435486A>G , CM000670.1:g.11435486A>G GRCh37
NC_000008.9:g.11472895A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_040035.1:n.784-393A>G