Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.169586497T= , CM000663.2:g.169586497T= | GRCh38 |
| NC_000001.10:g.169555735T= , CM000663.1:g.169555735T= | GRCh37 |
| NC_000001.9:g.167822359T= | NCBI36 |
| NG_011806.1:g.5035A= , LRG_553:g.5035A= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000367796.3:c.-111A= | ENSP00000356770.3:n.-111A= | |
| ENST00000367797.7:c.-111A= | ENSP00000356771.3:n.-111A= | |
| NM_000130.4:c.-111A= , LRG_553t1:c.-111A= | NP_000121.2:n.-111A= | |
| XM_017000660.2:c.-430A= | XP_016856149.1:n.-430A= |