Canonical Allele Identifier: CA535050371

Gene: LINC01104

Linked Data

• dbSNP Id: rs1489688653
• gnomAD v2: 2-100835695-G-T
• gnomAD v3: 2-100219233-G-T
• gnomAD v4: 2-100219233-G-T
• MyVariant Identifiers: chr2:g.100835695G>T (hg19) ; chr2:g.100219233G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.100219233G>T , CM000664.2:g.100219233G>T	GRCh38
NC_000002.11:g.100835695G>T , CM000664.1:g.100835695G>T	GRCh37
NC_000002.10:g.100202127G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_103730.1:n.567+10413G>T