Linked Data
gnomAD v4:
12-48981742-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.48981742C>T , CM000674.2:g.48981742C>T | GRCh38 |
| NC_000012.11:g.49375525C>T , CM000674.1:g.49375525C>T | GRCh37 |
| NC_000012.10:g.47661792C>T | NCBI36 |
| NG_033141.1:g.8290C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000293549.4:c.*102C>T MANE Select | ENSP00000293549.3:n.*102C>T | |
| NM_005430.3:c.*102C>T | NP_005421.1:n.*102C>T | |
| NM_005430.4:c.*102C>T MANE Select | NP_005421.1:n.*102C>T |