Canonical Allele Identifier: CA846958587
Gene: LINC02964 HGNC NCBI

Linked Data

dbSNP Id: rs1283155843
MyVariant Identifiers: chr8:g.126540029A>C (hg19) chr8:g.125527787A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.125527787A>C , CM000670.2:g.125527787A>C GRCh38
NC_000008.10:g.126540029A>C , CM000670.1:g.126540029A>C GRCh37
NC_000008.9:g.126609211A>C NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_928628.1:n.256+54473A>C
XR_001746072.1:n.583+4774A>C
XR_001746073.1:n.583+4774A>C
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