Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.119669632T= , CM000672.2:g.119669632T= | GRCh38 |
| NC_000010.10:g.121429144T= , CM000672.1:g.121429144T= | GRCh37 |
| NC_000010.9:g.121419134T= | NCBI36 |
| NG_016125.1:g.23263T= , LRG_742:g.23263T= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000369085.8:c.181-219T= MANE Select | ENSP00000358081.4:n.181-219T= | |
| ENST00000369085.7:c.181-219T= | ENSP00000358081.3:n.181-219T= | |
| ENST00000450186.1:c.7-219T= | ENSP00000410036.1:n.7-219T= | |
| NM_004281.3:c.181-219T= , LRG_742t1:c.181-219T= | NP_004272.2:n.181-219T= | |
| XM_005270287.1:c.181-219T= | XP_005270344.1:n.181-219T= | |
| XM_005270287.2:c.181-219T= | XP_005270344.1:n.181-219T= | |
| NM_004281.4:c.181-219T= MANE Select | NP_004272.2:n.181-219T= |