Canonical Allele Identifier: CA172383985
Gene: LINC00208 HGNC NCBI

Linked Data

dbSNP Id: rs377248267
gnomAD v2: 8-11435544-T-G
gnomAD v3: 8-11578035-T-G
gnomAD v4: 8-11578035-T-G

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.11578035T>G , CM000670.2:g.11578035T>G GRCh38
NC_000008.10:g.11435544T>G , CM000670.1:g.11435544T>G GRCh37
NC_000008.9:g.11472953T>G NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_040035.1:n.784-335T>G