Linked Data
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.47406694T>G , CM000666.2:g.47406694T>G | GRCh38 |
| NC_000004.11:g.47408711T>G , CM000666.1:g.47408711T>G | GRCh37 |
| NC_000004.10:g.47103468T>G | NCBI36 |
| NG_051831.1:g.380417T>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000295454.8:c.848T>G MANE Select | ENSP00000295454.3:p.Val283Gly | |
| ENST00000295454.7:c.848T>G | ENSP00000295454.3:p.Val283Gly | |
| NM_000812.3:c.848T>G | NP_000803.2:p.Val283Gly | |
| XM_011513678.1:c.827T>G | XP_011511980.1:p.Val276Gly | |
| XM_017007985.1:c.197T>G | XP_016863474.1:p.Val66Gly | |
| XM_024453976.1:c.749T>G | XP_024309744.1:p.Val250Gly | |
| XM_024453977.1:c.749T>G | XP_024309745.1:p.Val250Gly | |
| XM_024453978.1:c.749T>G | XP_024309746.1:p.Val250Gly | |
| NM_000812.4:c.848T>G MANE Select | NP_000803.2:p.Val283Gly |