Linked Data
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000022.11:g.50221279C>A , CM000684.2:g.50221279C>A | GRCh38 |
| NC_000022.10:g.50659708C>A , CM000684.1:g.50659708C>A | GRCh37 |
| NC_000022.9:g.49001835C>A | NCBI36 |
| NG_032160.1:g.28693G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000248846.10:c.3080G>T MANE Select | ENSP00000248846.5:p.Gly1027Val | |
| ENST00000248846.9:c.3080G>T | ENSP00000248846.5:p.Gly1027Val | |
| ENST00000439308.6:c.3080G>T | ENSP00000397387.2:p.Gly1027Val | |
| ENST00000491449.5:n.1387G>T | ||
| ENST00000498611.5:n.3613G>T | ||
| NM_020461.3:c.3080G>T | NP_065194.2:p.Gly1027Val | |
| XR_938347.1:n.3645G>T | ||
| XR_938348.1:n.3049+749G>T | ||
| XR_001755343.2:n.3649G>T | ||
| XR_001755344.2:n.3649G>T | ||
| XR_002958720.1:n.3053+749G>T | ||
| XR_938347.2:n.3649G>T | ||
| NM_020461.4:c.3080G>T MANE Select | NP_065194.3:p.Gly1027Val |