Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.159320334G= , CM000667.2:g.159320334G= | GRCh38 |
| NC_000005.9:g.158747342G= , CM000667.1:g.158747342G= | GRCh37 |
| NC_000005.8:g.158679920G= | NCBI36 |
| NG_009618.1:g.15140C= , LRG_71:g.15140C= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000696750.1:c.39C= | ENSP00000512849.1:p.Tyr13= | |
| ENST00000696751.1:c.*164C= | ENSP00000512850.1:n.*164C= | |
| ENST00000231228.3:c.669C= MANE Select | ENSP00000231228.2:p.Tyr223= | |
| ENST00000231228.2:c.669C= | ENSP00000231228.2:p.Tyr223= | |
| NM_002187.2:c.669C= , LRG_71t1:c.669C= | NP_002178.2:p.Tyr223= | |
| NM_002187.3:c.669C= MANE Select | NP_002178.2:p.Tyr223= |