Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.219418508C= , CM000664.2:g.219418508C= | GRCh38 |
| NC_000002.11:g.220283230C= , CM000664.1:g.220283230C= | GRCh37 |
| NC_000002.10:g.219991474C= | NCBI36 |
| NG_008043.1:g.5132C= , LRG_380:g.5132C= |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_001927.4:c.46C= MANE Select | NP_001918.3:p.Arg16= |
| ENST00000373960.4:c.46C= MANE Select | ENSP00000363071.3:p.Arg16= |
| NM_001382708.1:c.46C= | NP_001369637.1:p.Arg16= |
| NM_001382709.1:c.46C= | NP_001369638.1:p.Arg16= |
| NM_001382710.1:c.46C= | NP_001369639.1:p.Arg16= |
| NM_001382711.1:c.46C= | NP_001369640.1:p.Arg16= |
| NM_001382712.1:c.46C= | NP_001369641.1:p.Arg16= |
| NM_001382713.1:c.46C= | NP_001369642.1:p.Arg16= |
| NM_001927.3:c.46C= , LRG_380t1:c.46C= | NP_001918.3:p.Arg16= |
| ENST00000373960.3:c.46C= | ENSP00000363071.3:p.Arg16= |