Canonical Allele Identifier: CA213043481
Gene: LINC01475 HGNC NCBI

Linked Data

dbSNP Id: rs899441815

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.99527937A>T , CM000672.2:g.99527937A>T GRCh38
NC_000010.10:g.101287694A>T , CM000672.1:g.101287694A>T GRCh37
NC_000010.9:g.101277684A>T NCBI36
NG_016854.1:g.5A>T

Transcript Alleles

HGVS Amino-acid Change
NR_120618.1:n.446T>A