Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.33668974G= , CM000668.2:g.33668974G= | GRCh38 |
| NC_000006.11:g.33636751G= , CM000668.1:g.33636751G= | GRCh37 |
| NC_000006.10:g.33744729G= | NCBI36 |
| NG_027729.1:g.52596G= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000605930.3:c.2007G= MANE Select | ENSP00000475177.1:p.Glu669= | |
| ENST00000374316.9:c.2007G= | ENSP00000363435.4:p.Glu669= | |
| ENST00000605930.2:c.2007G= | ENSP00000475177.1:p.Glu669= | |
| NM_002224.3:c.2007G= | NP_002215.2:p.Glu669= | |
| XM_011514576.1:c.2076G= | XP_011512878.1:p.Glu692= | |
| XM_011514577.1:c.1824G= | XP_011512879.1:p.Glu608= | |
| XM_011514577.3:c.1824G= | XP_011512879.1:p.Glu608= | |
| XM_017010832.1:c.2007G= | XP_016866321.1:p.Glu669= | |
| NM_002224.4:c.2007G= MANE Select | NP_002215.2:p.Glu669= |