Canonical Allele Identifier: CA14641349
Gene: LINC01801 HGNC NCBI

Linked Data

dbSNP Id: rs1363364
gnomAD v2: 19-35308340-A-T
gnomAD v3: 19-34817436-A-T
gnomAD v4: 19-34817436-A-T
MyVariant Identifiers: chr19:g.35308340A>T (hg19) chr19:g.34817436A>T (hg38)
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'