Canonical Allele Identifier: CA337456663

Gene: LINC00278

Linked Data

• dbSNP Id: rs773537365
• gnomAD v3: Y-3004594-CT-C
• gnomAD v4: Y-3004594-CT-C
• MyVariant Identifiers: chrY:g.2872636del (hg19) ; chrY:g.3004595del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000024.10:g.3004595del , CM000686.2:g.3004595del	GRCh38
NC_000024.9:g.2872636del , CM000686.1:g.2872636del	GRCh37
NC_000024.8:g.2932636del	NCBI36

Transcript Alleles

HGVS	Amino-acid change
NR_046502.1:n.222+1378del