Canonical Allele Identifier: CA2722401460
Gene: LINC01475 HGNC NCBI

Linked Data

dbSNP Id: rs2119540786

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.99529090C>T , CM000672.2:g.99529090C>T GRCh38
NC_000010.10:g.101288847C>T , CM000672.1:g.101288847C>T GRCh37
NC_000010.9:g.101278837C>T NCBI36
NG_016854.1:g.1158C>T

Transcript Alleles

HGVS Amino-acid change
NR_120618.1:n.167-406G>A