Canonical Allele Identifier: CA253224647
Gene: LINC00331 HGNC NCBI

Linked Data

dbSNP Id: rs1016970741
MyVariant Identifiers: chr13:g.79410679A>G (hg19) chr13:g.78836544A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.78836544A>G , CM000675.2:g.78836544A>G GRCh38
NC_000013.10:g.79410679A>G , CM000675.1:g.79410679A>G GRCh37
NC_000013.9:g.78308680A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_046869.2:n.111+3396T>C
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