Canonical Allele Identifier: CA431149528
Gene: SNHG31 HGNC NCBI

Linked Data

gnomAD v4: 2-214810256-G-T
MyVariant Identifiers: chr2:g.215674980G>T (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.214810256G>T , CM000664.2:g.214810256G>T GRCh38
NC_000002.11:g.215674980G>T , CM000664.1:g.215674980G>T GRCh37
NC_000002.10:g.215383225G>T NCBI36
NG_012047.2:g.4449C>A
NG_012047.3:g.4456C>A

Transcript Alleles

HGVS Amino-acid Change
NR_110292.1:n.28G>T
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