Canonical Allele Identifier: CA580018057
Gene: LINC00208 HGNC NCBI

Linked Data

dbSNP Id: rs1229556788
gnomAD v2: 8-11435407-C-T
gnomAD v3: 8-11577898-C-T
gnomAD v4: 8-11577898-C-T

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.11577898C>T , CM000670.2:g.11577898C>T GRCh38
NC_000008.10:g.11435407C>T , CM000670.1:g.11435407C>T GRCh37
NC_000008.9:g.11472816C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_040035.1:n.784-472C>T