Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.35848389A= , CM000681.2:g.35848389A= | GRCh38 |
| NC_000019.9:g.36339291A= , CM000681.1:g.36339291A= | GRCh37 |
| NC_000019.8:g.41031131A= | NCBI36 |
| NG_013356.2:g.25899T= , LRG_693:g.25899T= | |
| NG_051206.1:g.1755A= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000378910.10:c.1179T= MANE Select | ENSP00000368190.4:p.His393= | |
| ENST00000353632.6:c.1179T= | ENSP00000343634.5:p.His393= | |
| ENST00000378910.9:c.1179T= | ENSP00000368190.4:p.His393= | |
| ENST00000592132.1:n.186T= | ||
| NM_004646.3:c.1179T= , LRG_693t1:c.1179T= | NP_004637.1:p.His393= | |
| NM_004646.4:c.1179T= MANE Select | NP_004637.1:p.His393= |