Canonical Allele Identifier: CA558962914
Gene: LINC02224 HGNC NCBI

Linked Data

dbSNP Id: rs1406379846
gnomAD v2: 5-44662573-G-T
gnomAD v3: 5-44662471-G-T
gnomAD v4: 5-44662471-G-T

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.44662471G>T , CM000667.2:g.44662471G>T GRCh38
NC_000005.9:g.44662573G>T , CM000667.1:g.44662573G>T GRCh37
NC_000005.8:g.44698330G>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_427699.2:n.92-3914C>A
XR_925983.1:n.71-3914C>A