Canonical Allele Identifier: CA1110700026
Gene: LINC00208 HGNC NCBI

Linked Data

dbSNP Id: rs1802024597
gnomAD v3: 8-11577826-G-C
gnomAD v4: 8-11577826-G-C
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.11577826G>C , CM000670.2:g.11577826G>C GRCh38
NC_000008.10:g.11435335G>C , CM000670.1:g.11435335G>C GRCh37
NC_000008.9:g.11472744G>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_040035.1:n.783+509G>C
Search 100 bp 5'
Search 100 bp 3'