Canonical Allele Identifier: CA471214076

Gene: LINC01475

Linked Data

• dbSNP Id: rs2033872419
• MyVariant Identifiers: chr10:g.101287668T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.99527911T>G , CM000672.2:g.99527911T>G	GRCh38
NC_000010.10:g.101287668T>G , CM000672.1:g.101287668T>G	GRCh37
NC_000010.9:g.101277658T>G	NCBI36

Transcript Alleles

HGVS	Amino-acid change
NR_120618.1:n.472A>C