Canonical Allele Identifier: CA223667973

Gene: SNHG1

Linked Data

• dbSNP Id: rs976241703
• MyVariant Identifiers: chr11:g.62622924A>C (hg19) ; chr11:g.62855452A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.62855452A>C , CM000673.2:g.62855452A>C	GRCh38
NC_000011.9:g.62622924A>C , CM000673.1:g.62622924A>C	GRCh37
NC_000011.8:g.62379500A>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_003098.1:n.39T>G
NR_003098.2:n.36T>G
NR_152575.1:n.434T>G
NR_152576.1:n.434T>G
NR_152577.1:n.36T>G
NR_152578.1:n.22-236T>G
NR_152579.1:n.36T>G
NR_152580.1:n.36T>G
NR_152581.1:n.36T>G
NR_152582.1:n.22-236T>G
NR_152583.1:n.36T>G
NR_152584.1:n.434T>G
NR_152585.1:n.434T>G