Linked Data
dbSNP Id:
rs1476837682
gnomAD v4:
3-87261967-G-GA
MyVariant Identifiers:
chr3:g.87311117_87311118insA (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.87261974dup , CM000665.2:g.87261974dup | GRCh38 |
| NC_000003.11:g.87311124dup , CM000665.1:g.87311124dup | GRCh37 |
| NC_000003.10:g.87393814dup | NCBI36 |
| NG_008225.2:g.19620dup |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000344265.8:c.682+103dup | ENSP00000342931.3:n.682+103dup | |
| ENST00000350375.7:c.604+103dup MANE Select | ENSP00000263781.2:n.604+103dup | |
| ENST00000344265.7:c.682+103dup | ENSP00000342931.3:n.682+103dup | |
| ENST00000350375.6:c.604+103dup | ENSP00000263781.2:n.604+103dup | |
| ENST00000560656.1:c.440-1864dup | ENSP00000452610.1:n.440-1864dup | |
| ENST00000561167.5:c.379+103dup | ENSP00000454072.1:n.379+103dup | |
| NM_000306.3:c.604+103dup | NP_000297.1:n.604+103dup | |
| NM_001122757.2:c.682+103dup | NP_001116229.1:n.682+103dup | |
| NM_000306.4:c.604+103dup MANE Select | NP_000297.1:n.604+103dup | |
| NM_001122757.3:c.682+103dup | NP_001116229.1:n.682+103dup |