Linked Data
gnomAD v4:
12-6016200-T-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.6016200T>C , CM000674.2:g.6016200T>C | GRCh38 |
| NC_000012.11:g.6125366T>C , CM000674.1:g.6125366T>C | GRCh37 |
| NC_000012.10:g.5995627T>C | NCBI36 |
| NG_009072.1:g.113471A>G | |
| NG_009072.2:g.113471A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000261405.10:c.5344A>G MANE Select | ENSP00000261405.5:p.Thr1782Ala | |
| ENST00000261405.9:c.5344A>G | ENSP00000261405.5:p.Thr1782Ala | |
| ENST00000538635.5:n.421-22266A>G | ||
| NM_000552.3:c.5344A>G | NP_000543.2:p.Thr1782Ala | |
| NM_000552.4:c.5344A>G | NP_000543.2:p.Thr1782Ala | |
| NM_000552.5:c.5344A>G MANE Select | NP_000543.3:p.Thr1782Ala |