Canonical Allele Identifier: CA2104288391
Gene: LINC00331 HGNC NCBI

Linked Data

dbSNP Id: rs1765202227
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Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.78836627A>C , CM000675.2:g.78836627A>C GRCh38
NC_000013.10:g.79410762A>C , CM000675.1:g.79410762A>C GRCh37
NC_000013.9:g.78308763A>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_046869.2:n.111+3313T>G
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Search 100 bp 3'