Canonical Allele Identifier: CA1817470641
Gene: LINC02964 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.125527885C= , CM000670.2:g.125527885C= GRCh38
NC_000008.10:g.126540127C= , CM000670.1:g.126540127C= GRCh37
NC_000008.9:g.126609309C= NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_928628.1:n.256+54571C=
XR_001746072.1:n.583+4872C=
XR_001746073.1:n.583+4872C=
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