Linked Data
gnomAD v4:
12-56042038-T-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.56042038T>G , CM000674.2:g.56042038T>G | GRCh38 |
| NC_000012.11:g.56435822T>G , CM000674.1:g.56435822T>G | GRCh37 |
| NC_000012.10:g.54722089T>G | NCBI36 |
| NG_023201.1:g.5137T>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000356464.10:c.-129T>G | ENSP00000348849.5:n.-129T>G | |
| ENST00000646449.2:c.-129T>G MANE Select | ENSP00000496643.1:n.-129T>G | |
| ENST00000356464.9:c.-129T>G | ENSP00000348849.5:n.-129T>G | |
| ENST00000552361.1:c.-61T>G | ENSP00000450339.1:n.-61T>G | |
| NM_001029.3:c.-129T>G | NP_001020.2:n.-129T>G | |
| NM_001029.5:c.-129T>G MANE Select | NP_001020.2:n.-129T>G |