Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.159323121A= , CM000667.2:g.159323121A= | GRCh38 |
| NC_000005.9:g.158750129A= , CM000667.1:g.158750129A= | GRCh37 |
| NC_000005.8:g.158682707A= | NCBI36 |
| NG_009618.1:g.12353T= , LRG_71:g.12353T= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000696750.1:c.-148-2601T= | ENSP00000512849.1:n.-148-2601T= | |
| ENST00000696751.1:c.297T= | ENSP00000512850.1:p.His99= | |
| ENST00000231228.3:c.297T= MANE Select | ENSP00000231228.2:p.His99= | |
| ENST00000231228.2:c.297T= | ENSP00000231228.2:p.His99= | |
| NM_002187.2:c.297T= , LRG_71t1:c.297T= | NP_002178.2:p.His99= | |
| XR_001742945.1:n.148-2413A= | ||
| NM_002187.3:c.297T= MANE Select | NP_002178.2:p.His99= |