Linked Data
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.129814213C>A , CM000671.2:g.129814213C>A | GRCh38 |
| NC_000009.11:g.132576492C>A , CM000671.1:g.132576492C>A | GRCh37 |
| NC_000009.10:g.131616313C>A | NCBI36 |
| NG_008049.1:g.14950G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000351698.5:c.758G>T MANE Select | ENSP00000345719.4:p.Trp253Leu | |
| ENST00000651202.1:c.*26G>T | ENSP00000498222.1:n.*26G>T | |
| ENST00000351698.4:c.758G>T | ENSP00000345719.4:p.Trp253Leu | |
| ENST00000474192.1:n.342G>T | ||
| NM_000113.2:c.758G>T | NP_000104.1:p.Trp253Leu | |
| XR_929731.1:n.1085G>T | ||
| XR_929731.3:n.953G>T | ||
| NM_000113.3:c.758G>T MANE Select | NP_000104.1:p.Trp253Leu |