Linked Data
gnomAD v4:
12-48981811-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.48981811C>T , CM000674.2:g.48981811C>T | GRCh38 |
| NC_000012.11:g.49375594C>T , CM000674.1:g.49375594C>T | GRCh37 |
| NC_000012.10:g.47661861C>T | NCBI36 |
| NG_033141.1:g.8359C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000293549.4:c.*171C>T MANE Select | ENSP00000293549.3:n.*171C>T | |
| NM_005430.3:c.*171C>T | NP_005421.1:n.*171C>T | |
| NM_005430.4:c.*171C>T MANE Select | NP_005421.1:n.*171C>T |