Canonical Allele Identifier: CA172383979
Gene: LINC00208 HGNC NCBI

Linked Data

dbSNP Id: rs913036479
gnomAD v2: 8-11435492-G-T
gnomAD v3: 8-11577983-G-T
gnomAD v4: 8-11577983-G-T

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.11577983G>T , CM000670.2:g.11577983G>T GRCh38
NC_000008.10:g.11435492G>T , CM000670.1:g.11435492G>T GRCh37
NC_000008.9:g.11472901G>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_040035.1:n.784-387G>T