Canonical Allele Identifier: CA87321038
Gene: LINC01322 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.165407371T>C , CM000665.2:g.165407371T>C GRCh38
NC_000003.11:g.165125159T>C , CM000665.1:g.165125159T>C GRCh37
NC_000003.10:g.166607853T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_125764.1:n.479+24464T>C
NR_125764.2:n.491+24464T>C
NR_174098.1:n.431+24412T>C
NR_174099.1:n.379+24464T>C
NR_174100.1:n.460+24464T>C
NR_174101.1:n.495+24412T>C
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