Canonical Allele Identifier: CA185516660
Gene: LINC02964 HGNC NCBI

Linked Data

dbSNP Id: rs1043145162
gnomAD v2: 8-126540019-C-T
gnomAD v3: 8-125527777-C-T
gnomAD v4: 8-125527777-C-T
MyVariant Identifiers: chr8:g.126540019C>T (hg19) chr8:g.125527777C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.125527777C>T , CM000670.2:g.125527777C>T GRCh38
NC_000008.10:g.126540019C>T , CM000670.1:g.126540019C>T GRCh37
NC_000008.9:g.126609201C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_928628.1:n.256+54463C>T
XR_001746072.1:n.583+4764C>T
XR_001746073.1:n.583+4764C>T
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