Linked Data
gnomAD v4:
11-6319261-G-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.6319261G>T , CM000673.2:g.6319261G>T | GRCh38 |
| NC_000011.9:g.6340491G>T , CM000673.1:g.6340491G>T | GRCh37 |
| NC_000011.8:g.6297067G>T | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000303927.4:c.688C>A MANE Select | ENSP00000307292.3:p.Pro230Thr | |
| ENST00000303927.3:c.688C>A | ENSP00000307292.3:p.Pro230Thr | |
| ENST00000524852.1:n.474C>A | ||
| ENST00000530979.1:c.784C>A | ENSP00000432047.1:p.Pro262Thr | |
| ENST00000532354.1:n.710C>A | ||
| NM_145040.2:c.688C>A | NP_659477.2:p.Pro230Thr | |
| XR_930997.1:n.720+1041G>T | ||
| XR_242848.4:n.121G>T | ||
| NM_145040.3:c.688C>A MANE Select | NP_659477.2:p.Pro230Thr |