Canonical Allele Identifier: CA471214116
Gene: LINC01475 HGNC NCBI

Linked Data

MyVariant Identifiers: chr10:g.101287682A>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.99527925A>G , CM000672.2:g.99527925A>G GRCh38
NC_000010.10:g.101287682A>G , CM000672.1:g.101287682A>G GRCh37
NC_000010.9:g.101277672A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_120618.1:n.458T>C