Canonical Allele Identifier: CA1118879522
Gene: LINC02964 HGNC NCBI

Linked Data

dbSNP Id: rs1813381813
gnomAD v3: 8-125527780-G-C
gnomAD v4: 8-125527780-G-C
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.125527780G>C , CM000670.2:g.125527780G>C GRCh38
NC_000008.10:g.126540022G>C , CM000670.1:g.126540022G>C GRCh37
NC_000008.9:g.126609204G>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_928628.1:n.256+54466G>C
XR_001746072.1:n.583+4767G>C
XR_001746073.1:n.583+4767G>C
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