Canonical Allele Identifier: CA846958492
Gene: LINC02964 HGNC NCBI

Linked Data

dbSNP Id: rs1288922653
MyVariant Identifiers: chr8:g.126539873G>T (hg19) chr8:g.125527631G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.125527631G>T , CM000670.2:g.125527631G>T GRCh38
NC_000008.10:g.126539873G>T , CM000670.1:g.126539873G>T GRCh37
NC_000008.9:g.126609055G>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_928628.1:n.256+54317G>T
XR_001746072.1:n.583+4618G>T
XR_001746073.1:n.583+4618G>T
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