Canonical Allele Identifier: CA1931371299
Gene: LINC01475 HGNC NCBI

Linked Data

dbSNP Id: rs2033872665

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.99527941_99527942insTATTACTTAAACA , CM000672.2:g.99527941_99527942insTATTACTTAAACA GRCh38
NC_000010.10:g.101287698_101287699insTATTACTTAAACA , CM000672.1:g.101287698_101287699insTATTACTTAAACA GRCh37
NC_000010.9:g.101277688_101277689insTATTACTTAAACA NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_120618.1:n.452_453insTATGTTTAAGTAA