Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.159320467C= , CM000667.2:g.159320467C= | GRCh38 |
| NC_000005.9:g.158747475C= , CM000667.1:g.158747475C= | GRCh37 |
| NC_000005.8:g.158680053C= | NCBI36 |
| NG_009618.1:g.15007G= , LRG_71:g.15007G= |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000696750.1:c.-95G= | ENSP00000512849.1:n.-95G= | |
| ENST00000696751.1:c.*31G= | ENSP00000512850.1:n.*31G= | |
| ENST00000231228.3:c.536G= MANE Select | ENSP00000231228.2:p.Arg179= | |
| ENST00000231228.2:c.536G= | ENSP00000231228.2:p.Arg179= | |
| NM_002187.2:c.536G= , LRG_71t1:c.536G= | NP_002178.2:p.Arg179= | |
| XR_001742945.1:n.18C= | ||
| NM_002187.3:c.536G= MANE Select | NP_002178.2:p.Arg179= |