Canonical Allele Identifier: CA431149684
Gene: SNHG31 HGNC NCBI

Linked Data

MyVariant Identifiers: chr2:g.215675015G>T (hg19)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.214810291G>T , CM000664.2:g.214810291G>T GRCh38
NC_000002.11:g.215675015G>T , CM000664.1:g.215675015G>T GRCh37
NC_000002.10:g.215383260G>T NCBI36
NG_012047.2:g.4414C>A
NG_012047.3:g.4421C>A

Transcript Alleles

HGVS Amino-acid Change
NR_110292.1:n.63G>T
Search 100 bp 5'
Search 100 bp 3'