Canonical Allele Identifier: CA1327085844
Gene: SNHG31 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.214810258A= , CM000664.2:g.214810258A= GRCh38
NC_000002.11:g.215674982A= , CM000664.1:g.215674982A= GRCh37
NC_000002.10:g.215383227A= NCBI36
NG_012047.2:g.4447T=
NG_012047.3:g.4454T=

Transcript Alleles

HGVS Amino-acid Change
NR_110292.1:n.30A=