Canonical Allele Identifier: CA2610478029
Gene: LINC01475 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.99527708A>G , CM000672.2:g.99527708A>G GRCh38
NC_000010.10:g.101287465A>G , CM000672.1:g.101287465A>G GRCh37
NC_000010.9:g.101277455A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_120618.1:n.577+98T>C