Canonical Allele Identifier: CA774555003

Gene: LINC01483

Linked Data

• dbSNP Id: rs1344523198
• gnomAD v3: 17-69854658-T-C
• gnomAD v4: 17-69854658-T-C
• MyVariant Identifiers: chr17:g.67850799T>C (hg19) ; chr17:g.69854658T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.69854658T>C , CM000679.2:g.69854658T>C	GRCh38
NC_000017.10:g.67850799T>C , CM000679.1:g.67850799T>C	GRCh37
NC_000017.9:g.65362394T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_109971.1:n.363+9172T>C
NR_109972.1:n.363+9172T>C