Linked Data
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.10115564G>T , CM000681.2:g.10115564G>T | GRCh38 |
| NC_000019.9:g.10226240G>T , CM000681.1:g.10226240G>T | GRCh37 |
| NC_000019.8:g.10087240G>T | NCBI36 |
| NG_047007.1:g.9044G>T | |
| NG_051197.1:g.9361C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000253108.9:c.862C>A MANE Select | ENSP00000253108.3:p.His288Asn | |
| ENST00000253108.8:c.862C>A | ENSP00000253108.3:p.His288Asn | |
| ENST00000589454.5:c.838C>A | ENSP00000466860.1:p.His280Asn | |
| ENST00000590158.1:n.881C>A | ||
| ENST00000593054.5:c.256C>A | ENSP00000467187.1:p.His86Asn | |
| NM_003755.3:c.862C>A | NP_003746.2:p.His288Asn | |
| NM_003755.4:c.862C>A | NP_003746.2:p.His288Asn | |
| NM_003755.5:c.862C>A MANE Select | NP_003746.2:p.His288Asn |