Canonical Allele Identifier: CA431149518
Gene: SNHG31 HGNC NCBI

Linked Data

dbSNP Id: rs144396879
gnomAD v3: 2-214810254-A-T
gnomAD v4: 2-214810254-A-T
MyVariant Identifiers: chr2:g.215674978A>T (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.214810254A>T , CM000664.2:g.214810254A>T GRCh38
NC_000002.11:g.215674978A>T , CM000664.1:g.215674978A>T GRCh37
NC_000002.10:g.215383223A>T NCBI36
NG_012047.2:g.4451T>A
NG_012047.3:g.4458T>A

Transcript Alleles

HGVS Amino-acid Change
NR_110292.1:n.26A>T
Search 100 bp 5'
Search 100 bp 3'