Linked Data
gnomAD v4:
3-10141765-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.10141765C>T , CM000665.2:g.10141765C>T | GRCh38 |
| NC_000003.11:g.10183449C>T , CM000665.1:g.10183449C>T | GRCh37 |
| NC_000003.10:g.10158449C>T | NCBI36 |
| NG_008212.3:g.5131C>T , LRG_322:g.5131C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000256474.2:c.-83C>T | ENSP00000256474.2:n.-83C>T | |
| NM_000551.3:c.-83C>T , LRG_322t1:c.-83C>T | NP_000542.1:n.-83C>T | |
| NM_198156.2:c.-83C>T | NP_937799.1:n.-83C>T | |
| XM_011534078.1:c.-83C>T | XP_011532380.1:n.-83C>T | |
| NM_001354723.1:c.-83C>T | NP_001341652.1:n.-83C>T |