Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.137199544C= , CM000671.2:g.137199544C= | GRCh38 |
| NC_000009.11:g.140093996C= , CM000671.1:g.140093996C= | GRCh37 |
| NC_000009.10:g.139213817C= | NCBI36 |
| NG_027801.1:g.6168G= | |
| NG_027801.2:g.9650G= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000409012.6:c.1168G= MANE Select | ENSP00000387100.4:p.Ala390= | |
| ENST00000333046.8:c.562G= | ENSP00000327617.4:p.Ala188= | |
| ENST00000409012.4:c.1168G= | ENSP00000387100.4:p.Ala390= | |
| ENST00000541945.1:n.90+4560G= | ||
| NM_001128228.2:c.1168G= | NP_001121700.2:p.Ala390= | |
| NM_001128228.3:c.1168G= MANE Select | NP_001121700.2:p.Ala390= |