Canonical Allele Identifier: CA471213812

Gene: LINC01475

Linked Data

• dbSNP Id: rs1312138975
• MyVariant Identifiers: chr10:g.101287578C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.99527821C>G , CM000672.2:g.99527821C>G	GRCh38
NC_000010.10:g.101287578C>G , CM000672.1:g.101287578C>G	GRCh37
NC_000010.9:g.101277568C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid change
NR_120618.1:n.562G>C