Canonical Allele Identifier: CA15633420

Gene: LINC01475

Linked Data

• dbSNP Id: rs12412391
• gnomAD v2: 10-101288935-A-G
• gnomAD v3: 10-99529178-A-G
• gnomAD v4: 10-99529178-A-G
• MyVariant Identifiers: chr10:g.101288935A>G (hg19) ; chr10:g.99529178A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.99529178A>G , CM000672.2:g.99529178A>G	GRCh38
NC_000010.10:g.101288935A>G , CM000672.1:g.101288935A>G	GRCh37
NC_000010.9:g.101278925A>G	NCBI36
NG_016854.1:g.1246A>G

Transcript Alleles

HGVS	Amino-acid change
NR_120618.1:n.167-494T>C