Canonical Allele Identifier: CA172383984
Gene: LINC00208 HGNC NCBI

Linked Data

dbSNP Id: rs937001625
MyVariant Identifiers: chr8:g.11578029C>T (hg38)

Genomic Alleles

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

Transcript Alleles

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