Canonical Allele Identifier: CA213043487
Gene: LINC01475 HGNC NCBI

Linked Data

dbSNP Id: rs1004812559

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.99528012T>C , CM000672.2:g.99528012T>C GRCh38
NC_000010.10:g.101287769T>C , CM000672.1:g.101287769T>C GRCh37
NC_000010.9:g.101277759T>C NCBI36
NG_016854.1:g.80T>C

Transcript Alleles

HGVS Amino-acid change
NR_120618.1:n.371A>G