Canonical Allele Identifier: CA471214091

Gene: LINC01475

Linked Data

• dbSNP Id: rs2033872446
• MyVariant Identifiers: chr10:g.101287673C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.99527916C>T , CM000672.2:g.99527916C>T	GRCh38
NC_000010.10:g.101287673C>T , CM000672.1:g.101287673C>T	GRCh37
NC_000010.9:g.101277663C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid change
NR_120618.1:n.467G>A