Canonical Allele Identifier: CA471214105
Gene: LINC01475 HGNC NCBI

Linked Data

MyVariant Identifiers: chr10:g.101287678C>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.99527921C>G , CM000672.2:g.99527921C>G GRCh38
NC_000010.10:g.101287678C>G , CM000672.1:g.101287678C>G GRCh37
NC_000010.9:g.101277668C>G NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_120618.1:n.462G>C