Canonical Allele Identifier: CA709158807

Gene: LINC02301

Linked Data

• dbSNP Id: rs1316950082
• gnomAD v3: 14-82739751-T-G
• gnomAD v4: 14-82739751-T-G
• MyVariant Identifiers: chr14:g.83206095T>G (hg19) ; chr14:g.82739751T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.82739751T>G , CM000676.2:g.82739751T>G	GRCh38
NC_000014.8:g.83206095T>G , CM000676.1:g.83206095T>G	GRCh37
NC_000014.7:g.82275848T>G	NCBI36

Transcript Alleles

HGVS	Amino-acid change
XR_944088.1:n.362-948T>G