Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000018.10:g.31530944T= , CM000680.2:g.31530944T= | GRCh38 |
| NC_000018.9:g.29110907T= , CM000680.1:g.29110907T= | GRCh37 |
| NC_000018.8:g.27364905T= | NCBI36 |
| NG_007072.3:g.37703T= , LRG_397:g.37703T= |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_001943.5:c.1015-43T= MANE Select | NP_001934.2:n.1015-43T= |
| ENST00000261590.13:c.1015-43T= MANE Select | ENSP00000261590.8:n.1015-43T= |
| NM_001943.3:c.1015-43T= , LRG_397t1:c.1015-43T= | NP_001934.2:n.1015-43T= |
| NM_001943.4:c.1015-43T= | NP_001934.2:n.1015-43T= |
| ENST00000261590.12:c.1015-43T= | ENSP00000261590.8:n.1015-43T= |
| ENST00000683614.1:c.846-43T= | |
| ENST00000683614.2:n.846-43T= | |
| XM_024451095.1:c.481-43T= | XP_024306863.1:n.481-43T= |