Linked Data
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.48974691C>A , CM000681.2:g.48974691C>A | GRCh38 |
| NC_000019.9:g.49477948C>A , CM000681.1:g.49477948C>A | GRCh37 |
| NC_000019.8:g.54169760C>A | NCBI36 |
| NG_012923.1:g.23663G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000323798.8:c.1351G>T MANE Select | ENSP00000317904.3:p.Asp451Tyr | |
| ENST00000263276.6:c.1159G>T | ENSP00000263276.6:p.Asp387Tyr | |
| ENST00000323798.7:c.1351G>T | ENSP00000317904.3:p.Asp451Tyr | |
| ENST00000472004.5:n.106G>T | ||
| ENST00000496048.1:n.258G>T | ||
| NM_001161587.1:c.1159G>T | NP_001155059.1:p.Asp387Tyr | |
| NM_002103.4:c.1351G>T | NP_002094.2:p.Asp451Tyr | |
| NR_027763.1:n.1410G>T | ||
| NM_002103.5:c.1351G>T MANE Select | NP_002094.2:p.Asp451Tyr | |
| NM_001161587.2:c.1159G>T | NP_001155059.1:p.Asp387Tyr | |
| NR_027763.2:n.1366G>T |