Canonical Allele Identifier: CA118203147
Gene: LINC02224 HGNC NCBI

Linked Data

dbSNP Id: rs937265719
gnomAD v3: 5-44662402-T-C
gnomAD v4: 5-44662402-T-C
MyVariant Identifiers: chr5:g.44662504T>C (hg19) chr5:g.44662402T>C (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.44662402T>C , CM000667.2:g.44662402T>C GRCh38
NC_000005.9:g.44662504T>C , CM000667.1:g.44662504T>C GRCh37
NC_000005.8:g.44698261T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_427699.2:n.92-3845A>G
XR_925983.1:n.71-3845A>G
Search 100 bp 5'
Search 100 bp 3'