Canonical Allele Identifier: CA431149524
Gene: SNHG31 HGNC NCBI

Linked Data

dbSNP Id: rs1177917967
MyVariant Identifiers: chr2:g.215674979T>A (hg19) chr2:g.214810255T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.214810255T>A , CM000664.2:g.214810255T>A GRCh38
NC_000002.11:g.215674979T>A , CM000664.1:g.215674979T>A GRCh37
NC_000002.10:g.215383224T>A NCBI36
NG_012047.2:g.4450A>T
NG_012047.3:g.4457A>T

Transcript Alleles

HGVS Amino-acid Change
NR_110292.1:n.27T>A
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