Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.173903885C= , CM000663.2:g.173903885C= | GRCh38 |
| NC_000001.10:g.173873023C= , CM000663.1:g.173873023C= | GRCh37 |
| NC_000001.9:g.172139646C= | NCBI36 |
| NG_012462.1:g.18494G= , LRG_577:g.18494G= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000367698.4:c.*4G= MANE Select | ENSP00000356671.3:n.*4G= | |
| ENST00000367698.3:c.*4G= | ENSP00000356671.3:n.*4G= | |
| ENST00000617423.4:c.*4G= | ENSP00000478688.1:n.*4G= | |
| NM_000488.3:c.*4G= , LRG_577t1:c.*4G= | NP_000479.1:n.*4G= | |
| XM_005245198.2:c.*4G= | XP_005245255.1:n.*4G= | |
| NM_001365052.1:c.*4G= | NP_001351981.1:n.*4G= | |
| NM_000488.4:c.*4G= MANE Select | NP_000479.1:n.*4G= | |
| NM_001365052.2:c.*4G= | NP_001351981.1:n.*4G= | |
| NM_001386302.1:c.*4G= | NP_001373231.1:n.*4G= | |
| NM_001386303.1:c.*4G= | NP_001373232.1:n.*4G= | |
| NM_001386304.1:c.*4G= | NP_001373233.1:n.*4G= | |
| NM_001386305.1:c.*4G= | NP_001373234.1:n.*4G= | |
| NM_001386306.1:c.*4G= | NP_001373235.1:n.*4G= |