Canonical Allele Identifier: CA580017993
Gene: LINC00208 HGNC NCBI

Linked Data

dbSNP Id: rs1206206904
gnomAD v2: 8-11435231-CCACAGTG-C
gnomAD v3: 8-11577722-CCACAGTG-C
gnomAD v4: 8-11577722-CCACAGTG-C
MyVariant Identifiers: chr8:g.11435232_11435238del (hg19) chr8:g.11577723_11577729del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.11577723_11577729del , CM000670.2:g.11577723_11577729del GRCh38
NC_000008.10:g.11435232_11435238del , CM000670.1:g.11435232_11435238del GRCh37
NC_000008.9:g.11472641_11472647del NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_040035.1:n.783+406_783+412del
Search 100 bp 5'
Search 100 bp 3'