Canonical Allele Identifier: CA1110700044
Gene: LINC00208 HGNC NCBI

Linked Data

dbSNP Id: rs1802025501
gnomAD v3: 8-11577863-A-G
gnomAD v4: 8-11577863-A-G
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.11577863A>G , CM000670.2:g.11577863A>G GRCh38
NC_000008.10:g.11435372A>G , CM000670.1:g.11435372A>G GRCh37
NC_000008.9:g.11472781A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_040035.1:n.784-507A>G
Search 100 bp 5'
Search 100 bp 3'