Canonical Allele Identifier: CA185516659
Gene: LINC02964 HGNC NCBI

Linked Data

dbSNP Id: rs946149165
gnomAD v2: 8-126540007-A-T
gnomAD v3: 8-125527765-A-T
gnomAD v4: 8-125527765-A-T
MyVariant Identifiers: chr8:g.126540007A>T (hg19) chr8:g.125527765A>T (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.125527765A>T , CM000670.2:g.125527765A>T GRCh38
NC_000008.10:g.126540007A>T , CM000670.1:g.126540007A>T GRCh37
NC_000008.9:g.126609189A>T NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_928628.1:n.256+54451A>T
XR_001746072.1:n.583+4752A>T
XR_001746073.1:n.583+4752A>T
Search 100 bp 5'
Search 100 bp 3'