Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.67940054C= , CM000678.2:g.67940054C= | GRCh38 |
| NC_000016.9:g.67973957C= , CM000678.1:g.67973957C= | GRCh37 |
| NC_000016.8:g.66531458C= | NCBI36 |
| NG_009778.1:g.9059G= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000264005.10:c.1173G= MANE Select | ENSP00000264005.5:p.Val391= | |
| ENST00000264005.9:c.1173G= | ENSP00000264005.5:p.Val391= | |
| ENST00000570369.5:c.176G= | ||
| ENST00000573538.5:c.911G= | ENSP00000463220.1:n.911G= | |
| NM_000229.1:c.1173G= | NP_000220.1:p.Val391= | |
| NM_000229.2:c.1173G= MANE Select | NP_000220.1:p.Val391= |