Canonical Allele Identifier: CA1118879525
Gene: LINC02964 HGNC NCBI

Linked Data

dbSNP Id: rs1813381887
gnomAD v3: 8-125527784-T-C
gnomAD v4: 8-125527784-T-C
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.125527784T>C , CM000670.2:g.125527784T>C GRCh38
NC_000008.10:g.126540026T>C , CM000670.1:g.126540026T>C GRCh37
NC_000008.9:g.126609208T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_928628.1:n.256+54470T>C
XR_001746072.1:n.583+4771T>C
XR_001746073.1:n.583+4771T>C
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