Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.32444611T= , CM000668.2:g.32444611T= | GRCh38 |
| NC_000006.11:g.32412388T= , CM000668.1:g.32412388T= | GRCh37 |
| NC_000006.10:g.32520366T= | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_019111.5:c.*12-41T= MANE Select | NP_061984.2:n.*12-41T= |
| ENST00000395388.7:c.*12-41T= MANE Select | ENSP00000378786.2:n.*12-41T= |
| NM_019111.4:c.*12-41T= | NP_061984.2:n.*12-41T= |
| ENST00000374982.5:c.*12-41T= | ENSP00000364121.5:n.*12-41T= |
| ENST00000395388.6:c.*12-41T= | ENSP00000378786.2:n.*12-41T= |