Canonical Allele Identifier: CA1327085860

Gene: SNHG31

Linked Data

• dbSNP Id: rs1696535352
• gnomAD v4: 2-214810291-GA-G

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.214810292del , CM000664.2:g.214810292del	GRCh38
NC_000002.11:g.215675016del , CM000664.1:g.215675016del	GRCh37
NC_000002.10:g.215383261del	NCBI36
NG_012047.2:g.4413del
NG_012047.3:g.4420del

Transcript Alleles

HGVS	Amino-acid Change
NR_110292.1:n.64del