Canonical Allele Identifier: CA471214141
Gene: LINC01475 HGNC NCBI

Linked Data

dbSNP Id: rs2033872704
MyVariant Identifiers: chr10:g.101287691C>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.99527934C>T , CM000672.2:g.99527934C>T GRCh38
NC_000010.10:g.101287691C>T , CM000672.1:g.101287691C>T GRCh37
NC_000010.9:g.101277681C>T NCBI36
NG_016854.1:g.2C>T

Transcript Alleles

HGVS Amino-acid Change
NR_120618.1:n.449G>A