Canonical Allele Identifier: CA2592729401
Gene: LINC00208 HGNC NCBI

Linked Data

dbSNP Id: rs2117643817
gnomAD v3: 8-11577869-C-T
gnomAD v4: 8-11577869-C-T

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.11577869C>T , CM000670.2:g.11577869C>T GRCh38
NC_000008.10:g.11435378C>T , CM000670.1:g.11435378C>T GRCh37
NC_000008.9:g.11472787C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_040035.1:n.784-501C>T