Linked Data
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.128304969T>G , CM000667.2:g.128304969T>G | GRCh38 |
| NC_000005.9:g.127640661T>G , CM000667.1:g.127640661T>G | GRCh37 |
| NC_000005.8:g.127668560T>G | NCBI36 |
| NG_008750.1:g.238075A>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000703783.1:n.2572A>C | ||
| ENST00000703785.1:n.2491A>C | ||
| ENST00000262464.9:c.5788A>C MANE Select | ENSP00000262464.4:p.Thr1930Pro | |
| ENST00000262464.8:c.5788A>C | ENSP00000262464.4:p.Thr1930Pro | |
| ENST00000508053.5:c.5788A>C | ENSP00000424571.1:p.Thr1930Pro | |
| ENST00000619499.4:c.5785A>C | ENSP00000482132.1:p.Thr1929Pro | |
| NM_001999.3:c.5788A>C | NP_001990.2:p.Thr1930Pro | |
| XM_017009228.2:c.5635A>C | XP_016864717.1:p.Thr1879Pro | |
| NM_001999.4:c.5788A>C MANE Select | NP_001990.2:p.Thr1930Pro |