Canonical Allele Identifier: CA337456661
Gene: LINC00278 HGNC NCBI

Linked Data

dbSNP Id: rs181063750
gnomAD v3: Y-3004569-C-A
gnomAD v4: Y-3004569-C-A
MyVariant Identifiers: chrY:g.2872610C>A (hg19) chrY:g.3004569C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.3004569C>A , CM000686.2:g.3004569C>A GRCh38
NC_000024.9:g.2872610C>A , CM000686.1:g.2872610C>A GRCh37
NC_000024.8:g.2932610C>A NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_046502.1:n.222+1352C>A
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