Linked Data
dbSNP Id:
rs1247053590
gnomAD v2:
11-121423731-GT-G
gnomAD v3:
11-121553022-GT-G
gnomAD v4:
11-121553022-GT-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.121553023del , CM000673.2:g.121553023del | GRCh38 |
| NC_000011.9:g.121423732del , CM000673.1:g.121423732del | GRCh37 |
| NC_000011.8:g.120928942del | NCBI36 |
| NG_023313.1:g.105772del |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000260197.12:c.2267-914del MANE Select | ENSP00000260197.6:n.2267-914del | |
| ENST00000260197.11:c.2267-914del | ENSP00000260197.6:n.2267-914del | |
| NM_003105.5:c.2267-914del | NP_003096.1:n.2267-914del | |
| XM_011542963.1:c.2267-914del | XP_011541265.1:n.2267-914del | |
| XM_011542964.1:c.2267-914del | XP_011541266.1:n.2267-914del | |
| XM_011542965.1:c.728-914del | XP_011541267.1:n.728-914del | |
| XM_011542963.3:c.2267-914del | XP_011541265.1:n.2267-914del | |
| XM_011542965.3:c.728-914del | XP_011541267.1:n.728-914del | |
| XM_017018169.2:c.1955-914del | XP_016873658.1:n.1955-914del | |
| XM_017018170.2:c.1742-914del | XP_016873659.1:n.1742-914del | |
| XM_017018171.1:c.2267-914del | XP_016873660.1:n.2267-914del | |
| XM_017018172.2:c.-282-914del | XP_016873661.1:n.-282-914del | |
| NM_003105.6:c.2267-914del MANE Select | NP_003096.2:n.2267-914del |