Linked Data
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.48974643T>A , CM000681.2:g.48974643T>A | GRCh38 |
| NC_000019.9:g.49477900T>A , CM000681.1:g.49477900T>A | GRCh37 |
| NC_000019.8:g.54169712T>A | NCBI36 |
| NG_012923.1:g.23711A>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000323798.8:c.1399A>T MANE Select | ENSP00000317904.3:p.Asn467Tyr | |
| ENST00000263276.6:c.1207A>T | ENSP00000263276.6:p.Asn403Tyr | |
| ENST00000323798.7:c.1399A>T | ENSP00000317904.3:p.Asn467Tyr | |
| ENST00000472004.5:n.154A>T | ||
| ENST00000496048.1:n.306A>T | ||
| NM_001161587.1:c.1207A>T | NP_001155059.1:p.Asn403Tyr | |
| NM_002103.4:c.1399A>T | NP_002094.2:p.Asn467Tyr | |
| NR_027763.1:n.1458A>T | ||
| NM_002103.5:c.1399A>T MANE Select | NP_002094.2:p.Asn467Tyr | |
| NM_001161587.2:c.1207A>T | NP_001155059.1:p.Asn403Tyr | |
| NR_027763.2:n.1414A>T |