Linked Data
gnomAD v4:
4-185143443-C-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.185143443C>G , CM000666.2:g.185143443C>G | GRCh38 |
| NC_000004.11:g.186064597C>G , CM000666.1:g.186064597C>G | GRCh37 |
| NC_000004.10:g.186301591C>G | NCBI36 |
| NG_013001.1:g.5181C>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000281456.11:c.71C>G MANE Select | ENSP00000281456.5:p.Thr24Ser | |
| ENST00000281456.10:c.71C>G | ENSP00000281456.5:p.Thr24Ser | |
| ENST00000491736.1:c.71C>G | ENSP00000476711.1:p.Thr24Ser | |
| NM_001151.3:c.71C>G | NP_001142.2:p.Thr24Ser | |
| NM_001151.4:c.71C>G MANE Select | NP_001142.2:p.Thr24Ser |