Canonical Allele Identifier: CA431149600
Gene: SNHG31 HGNC NCBI

Linked Data

MyVariant Identifiers: chr2:g.215674993A>T (hg19)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.214810269A>T , CM000664.2:g.214810269A>T GRCh38
NC_000002.11:g.215674993A>T , CM000664.1:g.215674993A>T GRCh37
NC_000002.10:g.215383238A>T NCBI36
NG_012047.2:g.4436T>A
NG_012047.3:g.4443T>A

Transcript Alleles

HGVS Amino-acid Change
NR_110292.1:n.41A>T
Search 100 bp 5'
Search 100 bp 3'