Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.186197059A>T , CM000666.2:g.186197059A>T | GRCh38 |
| NC_000004.11:g.187118213A>T , CM000666.1:g.187118213A>T | GRCh37 |
| NC_000004.10:g.187355207A>T | NCBI36 |
| NG_007965.1:g.10540A>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000378802.5:c.533A>T MANE Select | ENSP00000368079.4:p.Glu178Val | |
| ENST00000378802.4:c.533A>T | ENSP00000368079.4:p.Glu178Val | |
| ENST00000507209.5:n.972A>T | ||
| NM_207352.3:c.533A>T | NP_997235.3:p.Glu178Val | |
| XM_005262935.2:c.533A>T | XP_005262992.1:p.Glu178Val | |
| XM_006714184.2:c.137A>T | XP_006714247.1:p.Glu46Val | |
| XM_005262935.4:c.533A>T | XP_005262992.1:p.Glu178Val | |
| XM_017008037.1:c.137A>T | XP_016863526.1:p.Glu46Val | |
| NM_207352.4:c.533A>T MANE Select | NP_997235.3:p.Glu178Val |