Canonical Allele Identifier: CA471214099

Gene: LINC01475

Linked Data

• gnomAD v4: 10-99527919-T-C
• MyVariant Identifiers: chr10:g.101287676T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.99527919T>C , CM000672.2:g.99527919T>C	GRCh38
NC_000010.10:g.101287676T>C , CM000672.1:g.101287676T>C	GRCh37
NC_000010.9:g.101277666T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid change
NR_120618.1:n.464A>G