Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.169487739T= , CM000664.2:g.169487739T= | GRCh38 |
| NC_000002.11:g.170344249T= , CM000664.1:g.170344249T= | GRCh37 |
| NC_000002.10:g.170052495T= | NCBI36 |
| NG_011567.1:g.13244T= |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000295240.8:c.209-67T= MANE Select | ENSP00000295240.3:n.209-67T= | |
| ENST00000295240.7:c.209-67T= | ENSP00000295240.3:n.209-67T= | |
| ENST00000392663.6:c.209-67T= | ENSP00000376431.2:n.209-67T= | |
| ENST00000443151.1:c.143-248T= | ENSP00000406182.1:n.143-248T= | |
| ENST00000513963.1:c.209-67T= | ENSP00000424363.1:n.209-67T= | |
| NM_152384.2:c.209-67T= | NP_689597.1:n.209-67T= | |
| NM_152384.3:c.209-67T= MANE Select | NP_689597.1:n.209-67T= |