Canonical Allele Identifier: CA13200998

Gene: LINC01475

Linked Data

• dbSNP Id: rs6584283
• gnomAD v2: 10-101290301-T-C
• gnomAD v3: 10-99530544-T-C
• gnomAD v4: 10-99530544-T-C
• MyVariant Identifiers: chr10:g.101290301T>C (hg19) ; chr10:g.99530544T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.99530544T>C , CM000672.2:g.99530544T>C	GRCh38
NC_000010.10:g.101290301T>C , CM000672.1:g.101290301T>C	GRCh37
NC_000010.9:g.101280291T>C	NCBI36
NG_016854.1:g.2612T>C

Transcript Alleles

HGVS	Amino-acid change
NR_120618.1:n.166+468A>G