Canonical Allele Identifier: CA172383982
Gene: LINC00208 HGNC NCBI

Linked Data

dbSNP Id: rs116064466
gnomAD v2: 8-11435519-A-G
gnomAD v3: 8-11578010-A-G
gnomAD v4: 8-11578010-A-G

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.11578010A>G , CM000670.2:g.11578010A>G GRCh38
NC_000008.10:g.11435519A>G , CM000670.1:g.11435519A>G GRCh37
NC_000008.9:g.11472928A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_040035.1:n.784-360A>G