Canonical Allele Identifier: CA223668513
Gene: SNHG1 HGNC NCBI

Linked Data

dbSNP Id: rs890599067
gnomAD v2: 11-62623278-TAAAAG-T
gnomAD v3: 11-62855806-TAAAAG-T
gnomAD v4: 11-62855806-TAAAAG-T
MyVariant Identifiers: chr11:g.62623279_62623283del (hg19) chr11:g.62855807_62855811del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.62855811_62855815del , CM000673.2:g.62855811_62855815del GRCh38
NC_000011.9:g.62623283_62623287del , CM000673.1:g.62623283_62623287del GRCh37
NC_000011.8:g.62379859_62379863del NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_003098.1:n.24+54_24+58del
NR_003098.2:n.21+54_21+58del
NR_152575.1:n.75_79del
NR_152576.1:n.75_79del
NR_152577.1:n.21+54_21+58del
NR_152578.1:n.21+54_21+58del
NR_152579.1:n.21+54_21+58del
NR_152580.1:n.21+54_21+58del
NR_152581.1:n.21+54_21+58del
NR_152582.1:n.21+54_21+58del
NR_152583.1:n.21+54_21+58del
NR_152584.1:n.75_79del
NR_152585.1:n.75_79del
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