Canonical Allele Identifier: CA471213872

Gene: LINC01475

Linked Data

• gnomAD v4: 10-99527842-C-G
• MyVariant Identifiers: chr10:g.101287599C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.99527842C>G , CM000672.2:g.99527842C>G	GRCh38
NC_000010.10:g.101287599C>G , CM000672.1:g.101287599C>G	GRCh37
NC_000010.9:g.101277589C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid change
NR_120618.1:n.541G>C