Canonical Allele Identifier: CA213043469

Gene: LINC01475

Linked Data

• dbSNP Id: rs748021840
• gnomAD v2: 10-101287568-C-G
• gnomAD v3: 10-99527811-C-G
• gnomAD v4: 10-99527811-C-G
• MyVariant Identifiers: chr10:g.101287568C>G (hg19) ; chr10:g.99527811C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.99527811C>G , CM000672.2:g.99527811C>G	GRCh38
NC_000010.10:g.101287568C>G , CM000672.1:g.101287568C>G	GRCh37
NC_000010.9:g.101277558C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_120618.1:n.572G>C