Canonical Allele Identifier: CA431149662

Gene: SNHG31

Linked Data

• MyVariant Identifiers: chr2:g.215675008T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.214810284T>A , CM000664.2:g.214810284T>A	GRCh38
NC_000002.11:g.215675008T>A , CM000664.1:g.215675008T>A	GRCh37
NC_000002.10:g.215383253T>A	NCBI36
NG_012047.2:g.4421A>T
NG_012047.3:g.4428A>T

Transcript Alleles

HGVS	Amino-acid Change
NR_110292.1:n.56T>A