Canonical Allele Identifier: CA1763972771
Gene: LINC00208 HGNC NCBI

Linked Data

dbSNP Id: rs1585440773

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.11577710T>G , CM000670.2:g.11577710T>G GRCh38
NC_000008.10:g.11435219T>G , CM000670.1:g.11435219T>G GRCh37
NC_000008.9:g.11472628T>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_040035.1:n.783+393T>G