Canonical Allele Identifier: CA1327085828
Gene: SNHG31 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.214810232C= , CM000664.2:g.214810232C= GRCh38
NC_000002.11:g.215674956C= , CM000664.1:g.215674956C= GRCh37
NC_000002.10:g.215383201C= NCBI36
NG_012047.2:g.4473G=
NG_012047.3:g.4480G=

Transcript Alleles

HGVS Amino-acid Change
NR_110292.1:n.4C=