Linked Data
gnomAD v4:
12-48981669-G-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.48981669G>T , CM000674.2:g.48981669G>T | GRCh38 |
| NC_000012.11:g.49375452G>T , CM000674.1:g.49375452G>T | GRCh37 |
| NC_000012.10:g.47661719G>T | NCBI36 |
| NG_033141.1:g.8217G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000293549.4:c.*29G>T MANE Select | ENSP00000293549.3:n.*29G>T | |
| ENST00000293549.3:c.*29G>T | ENSP00000293549.3:n.*29G>T | |
| NM_005430.3:c.*29G>T | NP_005421.1:n.*29G>T | |
| NM_005430.4:c.*29G>T MANE Select | NP_005421.1:n.*29G>T |