Canonical Allele Identifier: CA185516668
Gene: LINC02964 HGNC NCBI

Linked Data

dbSNP Id: rs541311587
gnomAD v2: 8-126540063-GC-G
gnomAD v3: 8-125527821-GC-G
gnomAD v4: 8-125527821-GC-G
MyVariant Identifiers: chr8:g.126540064del (hg19) chr8:g.125527822del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.125527822del , CM000670.2:g.125527822del GRCh38
NC_000008.10:g.126540064del , CM000670.1:g.126540064del GRCh37
NC_000008.9:g.126609246del NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_928628.1:n.256+54508del
XR_001746072.1:n.583+4809del
XR_001746073.1:n.583+4809del
Search 100 bp 5'
Search 100 bp 3'