Canonical Allele Identifier: CA701182718
Gene: LINC00331 HGNC NCBI

Linked Data

dbSNP Id: rs1241520073
MyVariant Identifiers: chr13:g.79410657T>A (hg19) chr13:g.78836522T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.78836522T>A , CM000675.2:g.78836522T>A GRCh38
NC_000013.10:g.79410657T>A , CM000675.1:g.79410657T>A GRCh37
NC_000013.9:g.78308658T>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_046869.2:n.111+3418A>T
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