Canonical Allele Identifier: CA118203128
Gene: LINC02224 HGNC NCBI

Linked Data

dbSNP Id: rs189473044
gnomAD v3: 5-44662234-A-C
gnomAD v4: 5-44662234-A-C
MyVariant Identifiers: chr5:g.44662336A>C (hg19) chr5:g.44662234A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.44662234A>C , CM000667.2:g.44662234A>C GRCh38
NC_000005.9:g.44662336A>C , CM000667.1:g.44662336A>C GRCh37
NC_000005.8:g.44698093A>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_427699.2:n.92-3677T>G
XR_925983.1:n.71-3677T>G
Search 100 bp 5'
Search 100 bp 3'