Canonical Allele Identifier: CA985878195
Gene: LINC01483 HGNC NCBI

Linked Data

dbSNP Id: rs1917506816

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.69854694_69854695insCA , CM000679.2:g.69854694_69854695insCA GRCh38
NC_000017.10:g.67850835_67850836insCA , CM000679.1:g.67850835_67850836insCA GRCh37
NC_000017.9:g.65362430_65362431insCA NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_109971.1:n.363+9208_363+9209insCA
NR_109972.1:n.363+9208_363+9209insCA