Linked Data
dbSNP Id:
rs1721004446
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.55125324_55125325insGC , CM000666.2:g.55125324_55125325insGC | GRCh38 |
| NC_000004.11:g.55991491_55991492insGC , CM000666.1:g.55991491_55991492insGC | GRCh37 |
| NC_000004.10:g.55686248_55686249insGC | NCBI36 |
| NG_012004.1:g.5271_5272insGC |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000263923.5:c.-32_-31insGC MANE Select | ENSP00000263923.4:n.-32_-31insGC | |
| ENST00000263923.4:c.-32_-31insGC | ENSP00000263923.4:n.-32_-31insGC | |
| NM_002253.2:c.-32_-31insGC | NP_002244.1:n.-32_-31insGC | |
| NM_002253.3:c.-32_-31insGC | NP_002244.1:n.-32_-31insGC | |
| NM_002253.4:c.-32_-31insGC MANE Select | NP_002244.1:n.-32_-31insGC |