Canonical Allele Identifier: CA431149653

Gene: SNHG31

Linked Data

• MyVariant Identifiers: chr2:g.215675004A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.214810280A>C , CM000664.2:g.214810280A>C	GRCh38
NC_000002.11:g.215675004A>C , CM000664.1:g.215675004A>C	GRCh37
NC_000002.10:g.215383249A>C	NCBI36
NG_012047.2:g.4425T>G
NG_012047.3:g.4432T>G

Transcript Alleles

HGVS	Amino-acid Change
NR_110292.1:n.52A>C