Canonical Allele Identifier: CA471214382
Gene: LINC01475 HGNC NCBI

Linked Data

dbSNP Id: rs1322153874

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.99528017A>G , CM000672.2:g.99528017A>G GRCh38
NC_000010.10:g.101287774A>G , CM000672.1:g.101287774A>G GRCh37
NC_000010.9:g.101277764A>G NCBI36
NG_016854.1:g.85A>G

Transcript Alleles

HGVS Amino-acid change
NR_120618.1:n.366T>C