Canonical Allele Identifier: CA68163910

Gene: LINC01173

Linked Data

• dbSNP Id: rs4663476
• gnomAD v3: 2-234692420-T-A
• gnomAD v4: 2-234692420-T-A
• MyVariant Identifiers: chr2:g.235601064T>A (hg19) ; chr2:g.234692420T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.234692420T>A , CM000664.2:g.234692420T>A	GRCh38
NC_000002.11:g.235601064T>A , CM000664.1:g.235601064T>A	GRCh37
NC_000002.10:g.235265803T>A	NCBI36

Transcript Alleles

HGVS	Amino-acid change
NR_132376.1:n.102-3229T>A