Linked Data
dbSNP Id:
rs2109691616
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.40354149del , CM000666.2:g.40354149del | GRCh38 |
| NC_000004.11:g.40356166del , CM000666.1:g.40356166del | GRCh37 |
| NC_000004.10:g.40050923del | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000310169.3:c.1069del MANE Select | ENSP00000312663.2:p.Ser357AlafsTer26 | |
| ENST00000310169.2:c.1069del | ENSP00000312663.2:p.Ser357AlafsTer26 | |
| NM_017581.3:c.1069del | NP_060051.2:p.Ser357AlafsTer26 | |
| NM_017581.4:c.1069del MANE Select | NP_060051.2:p.Ser357AlafsTer26 |