Linked Data
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.129814199T>G , CM000671.2:g.129814199T>G | GRCh38 |
| NC_000009.11:g.132576478T>G , CM000671.1:g.132576478T>G | GRCh37 |
| NC_000009.10:g.131616299T>G | NCBI36 |
| NG_008049.1:g.14964A>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000351698.5:c.772A>C MANE Select | ENSP00000345719.4:p.Ile258Leu | |
| ENST00000651202.1:c.*40A>C | ENSP00000498222.1:n.*40A>C | |
| ENST00000351698.4:c.772A>C | ENSP00000345719.4:p.Ile258Leu | |
| ENST00000474192.1:n.356A>C | ||
| NM_000113.2:c.772A>C | NP_000104.1:p.Ile258Leu | |
| XR_929731.1:n.1099A>C | ||
| XR_929731.3:n.967A>C | ||
| NM_000113.3:c.772A>C MANE Select | NP_000104.1:p.Ile258Leu |