Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.96426858A= , CM000667.2:g.96426858A= | GRCh38 |
| NC_000005.9:g.95762562A= , CM000667.1:g.95762562A= | GRCh37 |
| NC_000005.8:g.95788318A= | NCBI36 |
| NG_021161.1:g.11424T= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000311106.8:c.286-928T= MANE Select | ENSP00000308024.2:n.286-928T= | |
| ENST00000311106.7:c.286-928T= | ENSP00000308024.2:n.286-928T= | |
| ENST00000508626.5:c.145-928T= | ENSP00000421600.1:n.145-928T= | |
| ENST00000509190.1:c.286-928T= | ENSP00000427294.1:n.286-928T= | |
| NM_000439.4:c.286-928T= | NP_000430.3:n.286-928T= | |
| NM_001177875.1:c.145-928T= | NP_001171346.1:n.145-928T= | |
| NR_130776.1:n.354+47206A= | ||
| NM_000439.5:c.286-928T= MANE Select | NP_000430.3:n.286-928T= | |
| NM_001177875.2:c.145-928T= | NP_001171346.1:n.145-928T= |