Canonical Allele Identifier: CA172383958

Gene: LINC00208

Linked Data

• dbSNP Id: rs537594656
• gnomAD v2: 8-11435362-C-T
• gnomAD v3: 8-11577853-C-T
• gnomAD v4: 8-11577853-C-T
• MyVariant Identifiers: chr8:g.11435362C>T (hg19) ; chr8:g.11577853C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.11577853C>T , CM000670.2:g.11577853C>T	GRCh38
NC_000008.10:g.11435362C>T , CM000670.1:g.11435362C>T	GRCh37
NC_000008.9:g.11472771C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_040035.1:n.784-517C>T