Canonical Allele Identifier: CA431149444

Gene: SNHG31

Linked Data

• gnomAD v4: 2-214810241-G-A
• MyVariant Identifiers: chr2:g.215674965G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.214810241G>A , CM000664.2:g.214810241G>A	GRCh38
NC_000002.11:g.215674965G>A , CM000664.1:g.215674965G>A	GRCh37
NC_000002.10:g.215383210G>A	NCBI36
NG_012047.2:g.4464C>T
NG_012047.3:g.4471C>T

Transcript Alleles

HGVS	Amino-acid Change
NR_110292.1:n.13G>A