Canonical Allele Identifier: CA213043471

Gene: LINC01475

Linked Data

• dbSNP Id: rs947310270
• gnomAD v3: 10-99527831-G-A
• gnomAD v4: 10-99527831-G-A
• MyVariant Identifiers: chr10:g.101287588G>A (hg19) ; chr10:g.99527831G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.99527831G>A , CM000672.2:g.99527831G>A	GRCh38
NC_000010.10:g.101287588G>A , CM000672.1:g.101287588G>A	GRCh37
NC_000010.9:g.101277578G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_120618.1:n.552C>T