Canonical Allele Identifier: CA627271658

Gene: LINC01483

Linked Data

• dbSNP Id: rs1263785343
• gnomAD v2: 17-67850830-A-G
• gnomAD v3: 17-69854689-A-G
• gnomAD v4: 17-69854689-A-G
• MyVariant Identifiers: chr17:g.67850830A>G (hg19) ; chr17:g.69854689A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.69854689A>G , CM000679.2:g.69854689A>G	GRCh38
NC_000017.10:g.67850830A>G , CM000679.1:g.67850830A>G	GRCh37
NC_000017.9:g.65362425A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_109971.1:n.363+9203A>G
NR_109972.1:n.363+9203A>G