Canonical Allele Identifier: CA474889025

Gene: SNHG1

Linked Data

• dbSNP Id: rs2085259340
• MyVariant Identifiers: chr11:g.62622558T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.62855086T>C , CM000673.2:g.62855086T>C	GRCh38
NC_000011.9:g.62622558T>C , CM000673.1:g.62622558T>C	GRCh37
NC_000011.8:g.62379134T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_003098.1:n.151+47A>G
NR_003098.2:n.148+47A>G
NR_152575.1:n.546+47A>G
NR_152576.1:n.538+47A>G
NR_152577.1:n.148+47A>G
NR_152578.1:n.105+47A>G
NR_152579.1:n.148+47A>G
NR_152580.1:n.148+47A>G
NR_152581.1:n.148+47A>G
NR_152582.1:n.105+47A>G
NR_152583.1:n.148+47A>G
NR_152584.1:n.546+47A>G
NR_152585.1:n.546+47A>G