Canonical Allele Identifier: CA471214078

Gene: LINC01475

Linked Data

• gnomAD v4: 10-99527912-A-G
• MyVariant Identifiers: chr10:g.101287669A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.99527912A>G , CM000672.2:g.99527912A>G	GRCh38
NC_000010.10:g.101287669A>G , CM000672.1:g.101287669A>G	GRCh37
NC_000010.9:g.101277659A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid change
NR_120618.1:n.471T>C