Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.43352768C= , CM000663.2:g.43352768C= | GRCh38 |
| NC_000001.10:g.43818439C= , CM000663.1:g.43818439C= | GRCh37 |
| NC_000001.9:g.43591026C= | NCBI36 |
| NG_007525.1:g.19965C= , LRG_510:g.19965C= |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_005373.3:c.1904C= MANE Select | NP_005364.1:p.Pro635= |
| ENST00000372470.9:c.1904C= MANE Select | ENSP00000361548.3:p.Pro635= |
| NM_005373.2:c.1904C= , LRG_510t1:c.1904C= | NP_005364.1:p.Pro635= |
| ENST00000372470.7:c.1904C= | ENSP00000361548.3:p.Pro635= |
| ENST00000413998.7:c.1883C= | ENSP00000414004.3:p.Pro628= |
| XM_011541478.1:c.1883C= | XP_011539780.1:p.Pro628= |
| XM_017001320.1:c.2075C= | XP_016856809.1:p.Pro692= |