Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.3595496G= , CM000681.2:g.3595496G= | GRCh38 |
| NC_000019.9:g.3595494G= , CM000681.1:g.3595494G= | GRCh37 |
| NC_000019.8:g.3546494G= | NCBI36 |
| NG_013363.1:g.16338C= , LRG_578:g.16338C= | |
| NG_031943.1:g.14926G= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000375190.10:c.*192C= MANE Select | ENSP00000364336.4:n.*192C= | |
| ENST00000375190.8:c.*192C= | ENSP00000364336.3:n.*192C= | |
| ENST00000411851.3:c.983+241C= | ENSP00000393333.2:n.983+241C= | |
| ENST00000589966.1:c.*55C= | ENSP00000468145.1:n.*55C= | |
| NM_001060.5:c.*192C= , LRG_578t1:c.*192C= | NP_001051.1:n.*192C= | |
| NM_201636.2:c.983+241C= | NP_963998.2:n.983+241C= | |
| NM_001060.6:c.*192C= MANE Select | NP_001051.1:n.*192C= | |
| NM_201636.3:c.983+241C= | NP_963998.2:n.983+241C= |