Canonical Allele Identifier: CA431149424
Gene: SNHG31 HGNC NCBI

Linked Data

MyVariant Identifiers: chr2:g.215674961C>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.214810237C>A , CM000664.2:g.214810237C>A GRCh38
NC_000002.11:g.215674961C>A , CM000664.1:g.215674961C>A GRCh37
NC_000002.10:g.215383206C>A NCBI36
NG_012047.2:g.4468G>T
NG_012047.3:g.4475G>T

Transcript Alleles

HGVS Amino-acid Change
NR_110292.1:n.9C>A
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