Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.64759690C= , CM000673.2:g.64759690C= | GRCh38 |
| NC_000011.9:g.64527162C= , CM000673.1:g.64527162C= | GRCh37 |
| NC_000011.8:g.64283738C= | NCBI36 |
| NG_013018.1:g.6026G= |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000164139.4:c.209G= MANE Select | ENSP00000164139.3:p.Arg70= | |
| ENST00000164139.3:c.209G= | ENSP00000164139.3:p.Arg70= | |
| ENST00000377432.7:c.209G= | ENSP00000366650.3:p.Arg70= | |
| NM_001164716.1:c.209G= | NP_001158188.1:p.Arg70= | |
| NM_005609.2:c.209G= | NP_005600.1:p.Arg70= | |
| NM_005609.3:c.209G= | NP_005600.1:p.Arg70= | |
| NM_005609.4:c.209G= MANE Select | NP_005600.1:p.Arg70= |