Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.42264802A= , CM000665.2:g.42264802A= | GRCh38 |
| NC_000003.11:g.42306294A= , CM000665.1:g.42306294A= | GRCh37 |
| NC_000003.10:g.42281298A= | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_000729.6:c.-108T= MANE Select | NP_000720.1:n.-108T= |
| ENST00000396169.7:c.-108T= MANE Select | ENSP00000379472.2:n.-108T= |
| NM_000729.4:c.-108T= | NP_000720.1:n.-108T= |
| NM_000729.5:c.-108T= | NP_000720.1:n.-108T= |
| ENST00000334681.9:c.-108T= | ENSP00000335657.5:n.-108T= |
| ENST00000396169.6:c.-108T= | ENSP00000379472.2:n.-108T= |