Canonical Allele Identifier: CA14641349
Gene: LINC01801 HGNC NCBI
MyVariant.info:
GRCh38 chr19:g.34817436A>T
GRCh37 chr19:g.35308340A>T
gnomAD v2:
19:35308340 A / T
gnomAD v3:
19:34817436 A / T
gnomAD v4:
chr19-34817436-A-T
Joint Max Group AF 0.68358334 (AFR)
Genomes Max Group AF 0.68358334 (AFR)
Exomes Max Group AF 0.47943527 (NFE)
dbSNP:
1363364
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.34817436A>T , CM000681.2:g.34817436A>T GRCh38
NC_000019.9:g.35308340A>T , CM000681.1:g.35308340A>T GRCh37
NC_000019.8:g.40000180A>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_033982.1:n.798T>A
Search 100 bp 5'
Search 100 bp 3'