Canonical Allele Identifier: CA185516646
Gene: LINC02964 HGNC NCBI

Linked Data

dbSNP Id: rs980142599
gnomAD v2: 8-126539837-T-C
gnomAD v3: 8-125527595-T-C
gnomAD v4: 8-125527595-T-C
MyVariant Identifiers: chr8:g.126539837T>C (hg19) chr8:g.125527595T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.125527595T>C , CM000670.2:g.125527595T>C GRCh38
NC_000008.10:g.126539837T>C , CM000670.1:g.126539837T>C GRCh37
NC_000008.9:g.126609019T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_928628.1:n.256+54281T>C
XR_001746072.1:n.583+4582T>C
XR_001746073.1:n.583+4582T>C
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