Canonical Allele Identifier: CA64811035
Gene: SNHG31 HGNC NCBI

Linked Data

dbSNP Id: rs1043418439
MyVariant Identifiers: chr2:g.215674961C>G (hg19) chr2:g.214810237C>G (hg38)
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Genomic Alleles

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

Transcript Alleles

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