Canonical Allele Identifier: CA431149413
Gene: SNHG31 HGNC NCBI

Linked Data

dbSNP Id: rs1696533411
gnomAD v3: 2-214810235-C-T
gnomAD v4: 2-214810235-C-T
MyVariant Identifiers: chr2:g.215674959C>T (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.214810235C>T , CM000664.2:g.214810235C>T GRCh38
NC_000002.11:g.215674959C>T , CM000664.1:g.215674959C>T GRCh37
NC_000002.10:g.215383204C>T NCBI36
NG_012047.2:g.4470G>A
NG_012047.3:g.4477G>A

Transcript Alleles

HGVS Amino-acid Change
NR_110292.1:n.7C>T
Search 100 bp 5'
Search 100 bp 3'