Canonical Allele Identifier: CA774555066

Gene: LINC01483

Linked Data

• dbSNP Id: rs1464498808
• MyVariant Identifiers: chr17:g.67851022G>T (hg19) ; chr17:g.69854881G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.69854881G>T , CM000679.2:g.69854881G>T	GRCh38
NC_000017.10:g.67851022G>T , CM000679.1:g.67851022G>T	GRCh37
NC_000017.9:g.65362617G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_109971.1:n.363+9395G>T
NR_109972.1:n.363+9395G>T