Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.128186633T= , CM000667.2:g.128186633T= | GRCh38 |
| NC_000005.9:g.127522325T= , CM000667.1:g.127522325T= | GRCh37 |
| NC_000005.8:g.127550224T= | NCBI36 |
| NG_042286.1:g.107843T= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000262461.7:c.*2T= MANE Select | ENSP00000262461.2:n.*2T= | |
| ENST00000262461.6:c.*2T= | ENSP00000262461.2:n.*2T= | |
| ENST00000343225.4:c.*2T= | ENSP00000340878.4:n.*2T= | |
| ENST00000509205.5:c.*254T= | ENSP00000427109.1:n.*254T= | |
| NM_001046.2:c.*2T= | NP_001037.1:n.*2T= | |
| NM_001256461.1:c.*2T= | NP_001243390.1:n.*2T= | |
| NR_046207.1:n.3871T= | ||
| XM_017009771.1:c.*2T= | XP_016865260.1:n.*2T= | |
| XR_001742214.1:n.3865T= | ||
| NM_001046.3:c.*2T= MANE Select | NP_001037.1:n.*2T= | |
| NM_001256461.2:c.*2T= | NP_001243390.1:n.*2T= | |
| NR_046207.2:n.3896T= |