Canonical Allele Identifier: CA337457600
Gene: LINC00278 HGNC NCBI
MyVariant.info:
GRCh38 chrY:g.3024109G>A
GRCh37 chrY:g.2892150G>A
gnomAD v3:
Y:3024109 G / A
gnomAD v4:
chrY-3024109-G-A
Joint Max Group AF 0.00278064 (NFE)
Genomes Max Group AF 0.00278064 (NFE)
dbSNP:
34738655
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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
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