Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.159320343A= , CM000667.2:g.159320343A= | GRCh38 |
| NC_000005.9:g.158747351A= , CM000667.1:g.158747351A= | GRCh37 |
| NC_000005.8:g.158679929A= | NCBI36 |
| NG_009618.1:g.15131T= , LRG_71:g.15131T= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000696750.1:c.30T= | ENSP00000512849.1:p.Tyr10= | |
| ENST00000696751.1:c.*155T= | ENSP00000512850.1:n.*155T= | |
| ENST00000231228.3:c.660T= MANE Select | ENSP00000231228.2:p.Tyr220= | |
| ENST00000231228.2:c.660T= | ENSP00000231228.2:p.Tyr220= | |
| NM_002187.2:c.660T= , LRG_71t1:c.660T= | NP_002178.2:p.Tyr220= | |
| NM_002187.3:c.660T= MANE Select | NP_002178.2:p.Tyr220= |