Canonical Allele Identifier: CA223668502

Gene: SNHG1

Linked Data

• dbSNP Id: rs536200130
• gnomAD v2: 11-62623240-C-T
• gnomAD v3: 11-62855768-C-T
• gnomAD v4: 11-62855768-C-T
• MyVariant Identifiers: chr11:g.62623240C>T (hg19) ; chr11:g.62855768C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.62855768C>T , CM000673.2:g.62855768C>T	GRCh38
NC_000011.9:g.62623240C>T , CM000673.1:g.62623240C>T	GRCh37
NC_000011.8:g.62379816C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_003098.1:n.24+97G>A
NR_003098.2:n.21+97G>A
NR_152575.1:n.118G>A
NR_152576.1:n.118G>A
NR_152577.1:n.21+97G>A
NR_152578.1:n.21+97G>A
NR_152579.1:n.21+97G>A
NR_152580.1:n.21+97G>A
NR_152581.1:n.21+97G>A
NR_152582.1:n.21+97G>A
NR_152583.1:n.21+97G>A
NR_152584.1:n.118G>A
NR_152585.1:n.118G>A