Canonical Allele Identifier: CA185516681
Gene: LINC02964 HGNC NCBI

Linked Data

dbSNP Id: rs762651355
gnomAD v2: 8-126540118-G-A
gnomAD v3: 8-125527876-G-A
gnomAD v4: 8-125527876-G-A
MyVariant Identifiers: chr8:g.126540118G>A (hg19) chr8:g.125527876G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.125527876G>A , CM000670.2:g.125527876G>A GRCh38
NC_000008.10:g.126540118G>A , CM000670.1:g.126540118G>A GRCh37
NC_000008.9:g.126609300G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_928628.1:n.256+54562G>A
XR_001746072.1:n.583+4863G>A
XR_001746073.1:n.583+4863G>A
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