Canonical Allele Identifier: CA627271638

Gene: LINC01483

Linked Data

• dbSNP Id: rs1303879886
• gnomAD v2: 17-67850579-T-G
• gnomAD v3: 17-69854438-T-G
• gnomAD v4: 17-69854438-T-G
• MyVariant Identifiers: chr17:g.67850579T>G (hg19) ; chr17:g.69854438T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.69854438T>G , CM000679.2:g.69854438T>G	GRCh38
NC_000017.10:g.67850579T>G , CM000679.1:g.67850579T>G	GRCh37
NC_000017.9:g.65362174T>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_109971.1:n.363+8952T>G
NR_109972.1:n.363+8952T>G