Canonical Allele Identifier: CA213043488
Gene: LINC01475 HGNC NCBI

Linked Data

dbSNP Id: rs112082268

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.99528015C>G , CM000672.2:g.99528015C>G GRCh38
NC_000010.10:g.101287772C>G , CM000672.1:g.101287772C>G GRCh37
NC_000010.9:g.101277762C>G NCBI36
NG_016854.1:g.83C>G

Transcript Alleles

HGVS Amino-acid change
NR_120618.1:n.368G>C