Canonical Allele Identifier: CA1817470529
Gene: LINC02964 HGNC NCBI

Linked Data

dbSNP Id: rs1813380203
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.125527668C>T , CM000670.2:g.125527668C>T GRCh38
NC_000008.10:g.126539910C>T , CM000670.1:g.126539910C>T GRCh37
NC_000008.9:g.126609092C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_928628.1:n.256+54354C>T
XR_001746072.1:n.583+4655C>T
XR_001746073.1:n.583+4655C>T
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