Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.15897471G= , CM000681.2:g.15897471G= | GRCh38 |
| NC_000019.9:g.16008281G= , CM000681.1:g.16008281G= | GRCh37 |
| NC_000019.8:g.15869281G= | NCBI36 |
| NG_007971.2:g.5604C= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000221700.11:c.141C= MANE Select | ENSP00000221700.3:p.Arg47= | |
| ENST00000011989.11:c.141C= | ENSP00000011989.8:p.Arg47= | |
| ENST00000221700.10:c.141C= | ENSP00000221700.3:p.Arg47= | |
| ENST00000392846.7:n.49+555C= | ||
| ENST00000586927.2:c.141C= | ENSP00000465514.1:p.Arg47= | |
| ENST00000587671.2:c.141C= | ENSP00000467443.2:p.Arg47= | |
| ENST00000608168.1:n.194C= | ||
| NM_001082.4:c.141C= | NP_001073.3:p.Arg47= | |
| NM_001082.5:c.141C= MANE Select | NP_001073.3:p.Arg47= |