Canonical Allele Identifier: CA337457600
Gene: LINC00278 HGNC NCBI

Linked Data

dbSNP Id: rs34738655
gnomAD v3: Y-3024109-G-A
gnomAD v4: Y-3024109-G-A
MyVariant Identifiers: chrY:g.2892150G>A (hg19) chrY:g.3024109G>A (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.3024109G>A , CM000686.2:g.3024109G>A GRCh38
NC_000024.9:g.2892150G>A , CM000686.1:g.2892150G>A GRCh37
NC_000024.8:g.2952150G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_046502.1:n.222+20892G>A
Search 100 bp 5'
Search 100 bp 3'