Linked Data
dbSNP Id:
rs1442709211
gnomAD v2:
12-103259614-AT-A
gnomAD v3:
12-102865836-AT-A
gnomAD v4:
12-102865836-AT-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.102865837del , CM000674.2:g.102865837del | GRCh38 |
| NC_000012.11:g.103259615del , CM000674.1:g.103259615del | GRCh37 |
| NC_000012.10:g.101783745del | NCBI36 |
| NG_008690.1:g.56766del | |
| NG_008690.2:g.97574del |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000553106.6:c.509+759del MANE Select | ENSP00000448059.1:n.509+759del | |
| ENST00000307000.7:c.494+759del | ENSP00000303500.2:n.494+759del | |
| ENST00000549111.5:n.605+759del | ||
| ENST00000551988.5:n.531-10505del | ||
| ENST00000553106.5:c.509+759del | ENSP00000448059.1:n.509+759del | |
| NM_000277.1:c.509+759del | NP_000268.1:n.509+759del | |
| XM_011538422.1:c.509+759del | XP_011536724.1:n.509+759del | |
| NM_000277.2:c.509+759del | NP_000268.1:n.509+759del | |
| NM_001354304.1:c.509+759del | NP_001341233.1:n.509+759del | |
| XM_017019370.2:c.509+759del | XP_016874859.1:n.509+759del | |
| NM_000277.3:c.509+759del MANE Select | NP_000268.1:n.509+759del | |
| NM_001354304.2:c.509+759del | NP_001341233.1:n.509+759del |