Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.46690812C= , CM000668.2:g.46690812C= | GRCh38 |
| NC_000006.11:g.46658549C= , CM000668.1:g.46658549C= | GRCh37 |
| NC_000006.10:g.46766508C= | NCBI36 |
| NG_051941.1:g.15545C= |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_001010870.3:c.2684C= MANE Select | NP_001010870.1:p.Pro895= |
| ENST00000316081.11:c.2684C= MANE Select | ENSP00000346065.5:p.Pro895= |
| NM_001010870.2:c.2684C= | NP_001010870.1:p.Pro895= |
| NM_001168359.1:c.2684C= | NP_001161831.1:p.Pro895= |
| NM_001168359.2:c.2684C= | NP_001161831.1:p.Pro895= |
| NR_144468.1:n.1373-5009C= | |
| NR_144468.2:n.1373-5009C= | |
| ENST00000316081.10:c.2684C= | ENSP00000346065.5:p.Pro895= |
| ENST00000544460.5:c.2684C= | ENSP00000443299.1:p.Pro895= |