Canonical Allele Identifier: CA811039993
Gene: LINC02224 HGNC NCBI

Linked Data

dbSNP Id: rs1333610015
gnomAD v3: 5-44662396-T-G
gnomAD v4: 5-44662396-T-G
MyVariant Identifiers: chr5:g.44662498T>G (hg19) chr5:g.44662396T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.44662396T>G , CM000667.2:g.44662396T>G GRCh38
NC_000005.9:g.44662498T>G , CM000667.1:g.44662498T>G GRCh37
NC_000005.8:g.44698255T>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_427699.2:n.92-3839A>C
XR_925983.1:n.71-3839A>C
Search 100 bp 5'
Search 100 bp 3'