Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.94942217A>T , CM000672.2:g.94942217A>T | GRCh38 |
| NC_000010.10:g.96701974A>T , CM000672.1:g.96701974A>T | GRCh37 |
| NC_000010.9:g.96691964A>T | NCBI36 |
| NG_008385.1:g.8560A>T | |
| NG_008385.2:g.9060A>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000260682.8:c.357A>T MANE Select | ENSP00000260682.6:p.Lys119Asn | |
| ENST00000643112.1:c.357A>T | ENSP00000496202.1:p.Lys119Asn | |
| ENST00000645207.1:n.510A>T | ||
| ENST00000260682.6:c.357A>T | ENSP00000260682.6:p.Lys119Asn | |
| ENST00000461906.1:n.382A>T | ||
| ENST00000473496.1:n.128A>T | ||
| NM_000771.3:c.357A>T | NP_000762.2:p.Lys119Asn | |
| NM_000771.4:c.357A>T MANE Select | NP_000762.2:p.Lys119Asn |