Canonical Allele Identifier: CA53081654

Gene: LINC01104

Linked Data

• dbSNP Id: rs980840511
• gnomAD v2: 2-100835717-C-A
• gnomAD v3: 2-100219255-C-A
• gnomAD v4: 2-100219255-C-A
• MyVariant Identifiers: chr2:g.100835717C>A (hg19) ; chr2:g.100219255C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.100219255C>A , CM000664.2:g.100219255C>A	GRCh38
NC_000002.11:g.100835717C>A , CM000664.1:g.100835717C>A	GRCh37
NC_000002.10:g.100202149C>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_103730.1:n.567+10435C>A