Canonical Allele Identifier: CA471213805

Gene: LINC01475

Linked Data

• gnomAD v4: 10-99527819-G-A
• MyVariant Identifiers: chr10:g.101287576G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.99527819G>A , CM000672.2:g.99527819G>A	GRCh38
NC_000010.10:g.101287576G>A , CM000672.1:g.101287576G>A	GRCh37
NC_000010.9:g.101277566G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_120618.1:n.564C>T