Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.94404736C= , CM000669.2:g.94404736C= | GRCh38 |
| NC_000007.13:g.94034048C= , CM000669.1:g.94034048C= | GRCh37 |
| NC_000007.12:g.93871984C= | NCBI36 |
| NG_007405.1:g.15176C= , LRG_2:g.15176C= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000297268.11:c.368C= MANE Select | ENSP00000297268.6:p.Pro123= | |
| ENST00000297268.10:c.368C= | ENSP00000297268.6:p.Pro123= | |
| ENST00000620463.1:c.362C= | ENSP00000477719.1:p.Pro121= | |
| NM_000089.3:c.368C= , LRG_2t1:c.368C= | NP_000080.2:p.Pro123= | |
| NM_000089.4:c.368C= MANE Select | NP_000080.2:p.Pro123= |