Canonical Allele Identifier: CA337457228
Gene: LINC00278 HGNC NCBI
dbSNP:
9786184
gnomAD v3:
Y:3019783 A / C
gnomAD v4:
chrY-3019783-A-C
Joint Max Group AF 0.95232103 (EAS)
Genomes Max Group AF 0.95232103 (EAS)
MyVariant.info:
GRCh38 chrY:g.3019783A>C
GRCh37 chrY:g.2887824A>C
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.3019783A>C , CM000686.2:g.3019783A>C GRCh38
NC_000024.9:g.2887824A>C , CM000686.1:g.2887824A>C GRCh37
NC_000024.8:g.2947824A>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_046502.1:n.222+16566A>C
Search 100 bp 5'
Search 100 bp 3'