Linked Data
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.841924G>T , CM000671.2:g.841924G>T | GRCh38 |
| NC_000009.11:g.841924G>T , CM000671.1:g.841924G>T | GRCh37 |
| NC_000009.10:g.831924G>T | NCBI36 |
| NG_009221.1:g.5235G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000382276.8:c.86G>T MANE Select | ENSP00000371711.3:p.Gly29Val | |
| ENST00000382276.7:c.86G>T | ENSP00000371711.3:p.Gly29Val | |
| ENST00000564322.1:n.235G>T | ||
| NM_021951.2:c.86G>T | NP_068770.2:p.Gly29Val | |
| XM_006716732.1:c.86G>T | XP_006716795.1:p.Gly29Val | |
| XM_017014375.1:c.86G>T | XP_016869864.1:p.Gly29Val | |
| NM_021951.3:c.86G>T MANE Select | NP_068770.2:p.Gly29Val |