Linked Data
dbSNP Id:
rs1557280334
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.50916216_50916217insTCC , CM000685.2:g.50916216_50916217insTCC | GRCh38 |
| NC_000023.10:g.50659216_50659217insTCC , CM000685.1:g.50659216_50659217insTCC | GRCh37 |
| NC_000023.9:g.50675956_50675957insTCC | NCBI36 |
| NG_012894.1:g.10433_10434insTCC |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000252677.4:c.788_789insTCC MANE Select | ENSP00000252677.3:p.Leu263_Arg264insPro | |
| ENST00000252677.3:c.788_789insTCC | ENSP00000252677.3:p.Leu263_Arg264insPro | |
| NM_005448.2:c.788_789insTCC MANE Select | NP_005439.2:p.Leu263_Arg264insPro |