Canonical Allele Identifier: CA118203144
Gene: LINC02224 HGNC NCBI

Linked Data

dbSNP Id: rs748077683
gnomAD v2: 5-44662488-C-T
gnomAD v3: 5-44662386-C-T
gnomAD v4: 5-44662386-C-T
MyVariant Identifiers: chr5:g.44662488C>T (hg19) chr5:g.44662386C>T (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.44662386C>T , CM000667.2:g.44662386C>T GRCh38
NC_000005.9:g.44662488C>T , CM000667.1:g.44662488C>T GRCh37
NC_000005.8:g.44698245C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_427699.2:n.92-3829G>A
XR_925983.1:n.71-3829G>A
Search 100 bp 5'
Search 100 bp 3'