Canonical Allele Identifier: CA938716374

Gene: SNHG1

Linked Data

• dbSNP Id: rs2085282779
• gnomAD v3: 11-62855547-A-AAG
• gnomAD v4: 11-62855547-A-AAG

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.62855547_62855548insAG , CM000673.2:g.62855547_62855548insAG	GRCh38
NC_000011.9:g.62623019_62623020insAG , CM000673.1:g.62623019_62623020insAG	GRCh37
NC_000011.8:g.62379595_62379596insAG	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_003098.1:n.25-82_25-81insCT
NR_003098.2:n.22-82_22-81insCT
NR_152575.1:n.338_339insCT
NR_152576.1:n.338_339insCT
NR_152577.1:n.22-82_22-81insCT
NR_152578.1:n.21+317_21+318insCT
NR_152579.1:n.22-82_22-81insCT
NR_152580.1:n.22-82_22-81insCT
NR_152581.1:n.22-82_22-81insCT
NR_152582.1:n.21+317_21+318insCT
NR_152583.1:n.22-82_22-81insCT
NR_152584.1:n.338_339insCT
NR_152585.1:n.338_339insCT