Canonical Allele Identifier: CA1763972936
Gene: LINC00208 HGNC NCBI

Linked Data

dbSNP Id: rs937001625

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.11578029C>G , CM000670.2:g.11578029C>G GRCh38
NC_000008.10:g.11435538C>G , CM000670.1:g.11435538C>G GRCh37
NC_000008.9:g.11472947C>G NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_040035.1:n.784-341C>G