Canonical Allele Identifier: CA1118879519
Gene: LINC02964 HGNC NCBI

Linked Data

dbSNP Id: rs1813381691
gnomAD v3: 8-125527771-A-G
gnomAD v4: 8-125527771-A-G
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.125527771A>G , CM000670.2:g.125527771A>G GRCh38
NC_000008.10:g.126540013A>G , CM000670.1:g.126540013A>G GRCh37
NC_000008.9:g.126609195A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_928628.1:n.256+54457A>G
XR_001746072.1:n.583+4758A>G
XR_001746073.1:n.583+4758A>G
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