Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.6592224C= , CM000671.2:g.6592224C= | GRCh38 |
| NC_000009.11:g.6592224C= , CM000671.1:g.6592224C= | GRCh37 |
| NC_000009.10:g.6582224C= | NCBI36 |
| NG_016397.1:g.58469G= , LRG_643:g.58469G= |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_000170.3:c.1402-1G= MANE Select | NP_000161.2:n.1402-1G= |
| ENST00000321612.8:c.1402-1G= MANE Select | ENSP00000370737.4:n.1402-1G= |
| NM_000170.2:c.1402-1G= , LRG_643t1:c.1402-1G= | NP_000161.2:n.1402-1G= |
| ENST00000321612.6:c.1402-1G= | ENSP00000370737.3:n.1402-1G= |
| ENST00000463305.1:n.486-1G= | |
| ENST00000639364.1:n.1102-1G= | |
| ENST00000639443.1:n.970-1G= | |
| ENST00000639954.1:n.1110-1G= | |
| ENST00000640592.1:n.1285-1G= | |
| ENST00000640703.1:n.245-1G= |