Linked Data
gnomAD v4:
9-133351771-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.133351771C>T , CM000671.2:g.133351771C>T | GRCh38 |
| NC_000009.10:g.135208447C>T | NCBI36 |
| NG_008477.1:g.9736G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000371974.8:c.*142G>A MANE Select | ENSP00000361042.3:n.*142G>A | |
| ENST00000371974.7:c.*142G>A | ENSP00000361042.3:n.*142G>A | |
| NM_003172.4:c.*142G>A MANE Select | NP_003163.1:n.*142G>A |