Canonical Allele Identifier: CA431149669

Gene: SNHG31

Linked Data

• dbSNP Id: rs1026104466
• gnomAD v2: 2-215675010-C-T
• gnomAD v3: 2-214810286-C-T
• gnomAD v4: 2-214810286-C-T
• MyVariant Identifiers: chr2:g.215675010C>T (hg19) ; chr2:g.214810286C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.214810286C>T , CM000664.2:g.214810286C>T	GRCh38
NC_000002.11:g.215675010C>T , CM000664.1:g.215675010C>T	GRCh37
NC_000002.10:g.215383255C>T	NCBI36
NG_012047.2:g.4419G>A
NG_012047.3:g.4426G>A

Transcript Alleles

HGVS	Amino-acid Change
NR_110292.1:n.58C>T