Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.142957798A= , CM000669.2:g.142957798A= | GRCh38 |
| NC_000007.13:g.142654885A= , CM000669.1:g.142654885A= | GRCh37 |
| NC_000007.12:g.142365007A= | NCBI36 |
| NG_007492.1:g.9619T= | |
| NG_007492.2:g.9619T= | |
| NG_007492.3:g.9619T= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000355265.7:c.672+29T= MANE Select | ENSP00000347409.2:n.672+29T= | |
| ENST00000355265.6:c.672+29T= | ENSP00000347409.2:n.672+29T= | |
| ENST00000476829.5:c.525+506T= | ENSP00000419889.1:n.525+506T= | |
| ENST00000479768.6:n.790+29T= | ||
| ENST00000494148.1:n.271+29T= | ||
| NM_000420.2:c.672+29T= | NP_000411.1:n.672+29T= | |
| XM_005249993.2:c.708+29T= | XP_005250050.1:n.708+29T= | |
| NM_000420.3:c.672+29T= MANE Select | NP_000411.1:n.672+29T= |