Canonical Allele Identifier: CA253224660
Gene: LINC00331 HGNC NCBI

Linked Data

dbSNP Id: rs1007529534
MyVariant Identifiers: chr13:g.79410772A>C (hg19) chr13:g.78836637A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.78836637A>C , CM000675.2:g.78836637A>C GRCh38
NC_000013.10:g.79410772A>C , CM000675.1:g.79410772A>C GRCh37
NC_000013.9:g.78308773A>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_046869.2:n.111+3303T>G
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