Canonical Allele Identifier: CA53081627

Gene: LINC01104

Linked Data

• dbSNP Id: rs558276199
• gnomAD v2: 2-100835622-TCTC-T
• gnomAD v3: 2-100219160-TCTC-T
• gnomAD v4: 2-100219160-TCTC-T
• MyVariant Identifiers: chr2:g.100835623_100835625del (hg19) ; chr2:g.100219161_100219163del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.100219164_100219166del , CM000664.2:g.100219164_100219166del	GRCh38
NC_000002.11:g.100835626_100835628del , CM000664.1:g.100835626_100835628del	GRCh37
NC_000002.10:g.100202058_100202060del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_103730.1:n.567+10344_567+10346del