Canonical Allele Identifier: CA172383978
Gene: LINC00208 HGNC NCBI

Linked Data

dbSNP Id: rs142069021
gnomAD v3: 8-11577955-G-C
gnomAD v4: 8-11577955-G-C
MyVariant Identifiers: chr8:g.11435464G>C (hg19) chr8:g.11577955G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.11577955G>C , CM000670.2:g.11577955G>C GRCh38
NC_000008.10:g.11435464G>C , CM000670.1:g.11435464G>C GRCh37
NC_000008.9:g.11472873G>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_040035.1:n.784-415G>C
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