Canonical Allele Identifier: CA337458232
Gene: LINC00278 HGNC NCBI

Linked Data

dbSNP Id: rs9786252
gnomAD v3: Y-3042992-G-A
gnomAD v4: Y-3042992-G-A
MyVariant Identifiers: chrY:g.2911033G>A (hg19) chrY:g.3042992G>A (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.3042992G>A , CM000686.2:g.3042992G>A GRCh38
NC_000024.9:g.2911033G>A , CM000686.1:g.2911033G>A GRCh37
NC_000024.8:g.2971033G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_046502.1:n.223-36292G>A
Search 100 bp 5'
Search 100 bp 3'