Canonical Allele Identifier: CA118203151

Gene: LINC02224

Linked Data

• dbSNP Id: rs947447825
• gnomAD v2: 5-44662527-A-C
• gnomAD v3: 5-44662425-A-C
• gnomAD v4: 5-44662425-A-C
• MyVariant Identifiers: chr5:g.44662527A>C (hg19) ; chr5:g.44662425A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.44662425A>C , CM000667.2:g.44662425A>C	GRCh38
NC_000005.9:g.44662527A>C , CM000667.1:g.44662527A>C	GRCh37
NC_000005.8:g.44698284A>C	NCBI36

Transcript Alleles

HGVS	Amino-acid change
XR_427699.2:n.92-3868T>G
XR_925983.1:n.71-3868T>G