Canonical Allele Identifier: CA2589166947

Gene: LINC01153

Linked Data

• dbSNP Id: rs2133945547
• gnomAD v3: 10-121179911-T-G
• gnomAD v4: 10-121179911-T-G

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.121179911T>G , CM000672.2:g.121179911T>G	GRCh38
NC_000010.10:g.122939425T>G , CM000672.1:g.122939425T>G	GRCh37
NC_000010.9:g.122929415T>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_246197.2:n.684+939T>G