Canonical Allele Identifier: CA53081623

Gene: LINC01104

Linked Data

• dbSNP Id: rs980650601
• gnomAD v2: 2-100835603-G-C
• gnomAD v3: 2-100219141-G-C
• gnomAD v4: 2-100219141-G-C
• MyVariant Identifiers: chr2:g.100835603G>C (hg19) ; chr2:g.100219141G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.100219141G>C , CM000664.2:g.100219141G>C	GRCh38
NC_000002.11:g.100835603G>C , CM000664.1:g.100835603G>C	GRCh37
NC_000002.10:g.100202035G>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_103730.1:n.567+10321G>C