Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.6595175T= , CM000671.2:g.6595175T= | GRCh38 |
| NC_000009.11:g.6595175T= , CM000671.1:g.6595175T= | GRCh37 |
| NC_000009.10:g.6585175T= | NCBI36 |
| NG_016397.1:g.55518A= , LRG_643:g.55518A= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000321612.8:c.1156-56A= MANE Select | ENSP00000370737.4:n.1156-56A= | |
| ENST00000638654.1:c.403-56A= | ENSP00000491101.1:n.403-56A= | |
| ENST00000639364.1:n.856-56A= | ||
| ENST00000639443.1:n.724-56A= | ||
| ENST00000639493.1:n.308-56A= | ||
| ENST00000639954.1:n.864-56A= | ||
| ENST00000640592.1:n.1039-56A= | ||
| ENST00000321612.6:c.1156-56A= | ENSP00000370737.3:n.1156-56A= | |
| ENST00000463305.1:n.240-56A= | ||
| NM_000170.2:c.1156-56A= , LRG_643t1:c.1156-56A= | NP_000161.2:n.1156-56A= | |
| NM_000170.3:c.1156-56A= MANE Select | NP_000161.2:n.1156-56A= |