Linked Data
gnomAD v4:
13-53051674-T-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000013.11:g.53051674T>C , CM000675.2:g.53051674T>C | GRCh38 |
| NC_000013.10:g.53625809T>C , CM000675.1:g.53625809T>C | GRCh37 |
| NC_000013.9:g.52523810T>C | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000219022.3:c.*903T>C MANE Select | ENSP00000219022.2:n.*903T>C | |
| ENST00000219022.2:c.*903T>C | ENSP00000219022.2:n.*903T>C | |
| NM_006418.4:c.*903T>C | NP_006409.3:n.*903T>C | |
| NM_006418.5:c.*903T>C MANE Select | NP_006409.3:n.*903T>C |