Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.80675169T= , CM000667.2:g.80675169T= | GRCh38 |
| NC_000005.9:g.79970988T= , CM000667.1:g.79970988T= | GRCh37 |
| NC_000005.8:g.80006744T= | NCBI36 |
| NG_016607.1:g.25695T= | |
| NG_016607.2:g.25695T= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000265081.7:c.1173+41T= MANE Select | ENSP00000265081.6:n.1173+41T= | |
| ENST00000658259.1:c.1005+41T= | ENSP00000499617.1:n.1005+41T= | |
| ENST00000667069.1:c.1173+41T= | ENSP00000499502.1:n.1173+41T= | |
| ENST00000670357.1:c.1173+41T= | ENSP00000499791.1:n.1173+41T= | |
| ENST00000265081.6:c.1173+41T= | ENSP00000265081.6:n.1173+41T= | |
| NM_002439.4:c.1173+41T= | NP_002430.3:n.1173+41T= | |
| NM_002439.5:c.1173+41T= MANE Select | NP_002430.3:n.1173+41T= |