Linked Data
gnomAD v4:
10-113588561-T-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.113588561T>G , CM000672.2:g.113588561T>G | GRCh38 |
| NC_000010.10:g.115348320T>G , CM000672.1:g.115348320T>G | GRCh37 |
| NC_000010.9:g.115338310T>G | NCBI36 |
| NG_008956.1:g.40543T>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000351270.4:c.*192T>G MANE Select | ENSP00000277903.4:n.*192T>G | |
| ENST00000351270.3:c.*192T>G | ENSP00000277903.4:n.*192T>G | |
| ENST00000542051.5:c.*192T>G | ENSP00000443283.1:n.*192T>G | |
| NM_001177660.1:c.*192T>G | NP_001171131.1:n.*192T>G | |
| NM_004132.3:c.*192T>G | NP_004123.1:n.*192T>G | |
| NM_001177660.2:c.*192T>G | NP_001171131.1:n.*192T>G | |
| NM_004132.4:c.*192T>G | NP_004123.1:n.*192T>G | |
| NM_004132.5:c.*192T>G MANE Select | NP_004123.1:n.*192T>G | |
| NM_001177660.3:c.*192T>G | NP_001171131.1:n.*192T>G |