Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.81207031T= , CM000667.2:g.81207031T= | GRCh38 |
| NC_000005.9:g.80502850T= , CM000667.1:g.80502850T= | GRCh37 |
| NC_000005.8:g.80538606T= | NCBI36 |
| NG_030334.1:g.251343T= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000265080.9:c.2967+126T= MANE Select | ENSP00000265080.4:n.2967+126T= | |
| ENST00000265080.8:c.2967+126T= | ENSP00000265080.4:n.2967+126T= | |
| ENST00000503795.1:c.2967+126T= | ENSP00000421771.1:n.2967+126T= | |
| NM_006909.2:c.2967+126T= | NP_008840.1:n.2967+126T= | |
| XM_017009682.2:c.2682+126T= | XP_016865171.1:n.2682+126T= | |
| XR_002956166.1:n.3083+126T= | ||
| NM_006909.3:c.2967+126T= MANE Select | NP_008840.1:n.2967+126T= |