Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.30737381A= , CM000678.2:g.30737381A= | GRCh38 |
| NC_000016.9:g.30748702A= , CM000678.1:g.30748702A= | GRCh37 |
| NC_000016.8:g.30656203A= | NCBI36 |
| NG_032135.1:g.43241A= |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000411466.7:c.7341A= | ENSP00000405186.3:p.Pro2447= | |
| ENST00000704023.1:c.1593+28A= | ||
| ENST00000706321.1:c.7341A= | ENSP00000516346.1:p.Pro2447= | |
| ENST00000262518.9:c.7341A= MANE Select | ENSP00000262518.4:p.Pro2447= | |
| ENST00000262518.8:c.7341A= | ENSP00000262518.4:p.Pro2447= | |
| ENST00000380361.7:c.6810A= | ENSP00000369719.3:p.Pro2270= | |
| ENST00000395059.6:c.6564A= | ENSP00000378499.3:p.Pro2188= | |
| NM_006662.2:c.7341A= | NP_006653.2:p.Pro2447= | |
| NM_006662.3:c.7341A= MANE Select | NP_006653.2:p.Pro2447= |