Canonical Allele Identifier: CA64811042
Gene: SNHG31 HGNC NCBI

Linked Data

dbSNP Id: rs536755691
gnomAD v3: 2-214810244-G-A
gnomAD v4: 2-214810244-G-A
MyVariant Identifiers: chr2:g.215674968G>A (hg19) chr2:g.214810244G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.214810244G>A , CM000664.2:g.214810244G>A GRCh38
NC_000002.11:g.215674968G>A , CM000664.1:g.215674968G>A GRCh37
NC_000002.10:g.215383213G>A NCBI36
NG_012047.2:g.4461C>T
NG_012047.3:g.4468C>T

Transcript Alleles

HGVS Amino-acid Change
NR_110292.1:n.16G>A
Search 100 bp 5'
Search 100 bp 3'