Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.99307694T= , CM000666.2:g.99307694T= | GRCh38 |
| NC_000004.11:g.100228851T= , CM000666.1:g.100228851T= | GRCh37 |
| NC_000004.10:g.100447874T= | NCBI36 |
| NG_011435.1:g.18722A= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000305046.13:c.*146A= MANE Select | ENSP00000306606.8:n.*146A= | |
| ENST00000305046.12:c.*146A= | ENSP00000306606.8:n.*146A= | |
| ENST00000506651.5:c.*146A= | ENSP00000425998.2:n.*146A= | |
| ENST00000515694.4:n.3369A= | ||
| ENST00000625860.2:c.*146A= | ENSP00000486614.1:n.*146A= | |
| NM_000668.5:c.*146A= | NP_000659.2:n.*146A= | |
| NM_001286650.1:c.*146A= | NP_001273579.1:n.*146A= | |
| NM_000668.6:c.*146A= MANE Select | NP_000659.2:n.*146A= | |
| NM_001286650.2:c.*146A= | NP_001273579.1:n.*146A= |