Canonical Allele Identifier: CA1075652841
Gene: LINC02224 HGNC NCBI

Linked Data

dbSNP Id: rs1739807608
gnomAD v3: 5-44662347-C-T
gnomAD v4: 5-44662347-C-T

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.44662347C>T , CM000667.2:g.44662347C>T GRCh38
NC_000005.9:g.44662449C>T , CM000667.1:g.44662449C>T GRCh37
NC_000005.8:g.44698206C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_427699.2:n.92-3790G>A
XR_925983.1:n.71-3790G>A