Linked Data
gnomAD v4:
10-113588413-T-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.113588413T>C , CM000672.2:g.113588413T>C | GRCh38 |
| NC_000010.10:g.115348172T>C , CM000672.1:g.115348172T>C | GRCh37 |
| NC_000010.9:g.115338162T>C | NCBI36 |
| NG_008956.1:g.40395T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000351270.4:c.*44T>C MANE Select | ENSP00000277903.4:n.*44T>C | |
| ENST00000351270.3:c.*44T>C | ENSP00000277903.4:n.*44T>C | |
| ENST00000542051.5:c.*44T>C | ENSP00000443283.1:n.*44T>C | |
| NM_001177660.1:c.*44T>C | NP_001171131.1:n.*44T>C | |
| NM_004132.3:c.*44T>C | NP_004123.1:n.*44T>C | |
| NM_001177660.2:c.*44T>C | NP_001171131.1:n.*44T>C | |
| NM_004132.4:c.*44T>C | NP_004123.1:n.*44T>C | |
| NM_004132.5:c.*44T>C MANE Select | NP_004123.1:n.*44T>C | |
| NM_001177660.3:c.*44T>C | NP_001171131.1:n.*44T>C |