Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.114716123C= , CM000663.2:g.114716123C= | GRCh38 |
| NC_000001.10:g.115258744C= , CM000663.1:g.115258744C= | GRCh37 |
| NC_000001.9:g.115060267C= | NCBI36 |
| NG_007572.1:g.5772G= , LRG_92:g.5772G= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000369535.5:c.38G= MANE Select | ENSP00000358548.4:p.Gly13= | |
| ENST00000369535.4:c.38G= | ENSP00000358548.4:p.Gly13= | |
| NM_002524.4:c.38G= | NP_002515.1:p.Gly13= | |
| NM_002524.5:c.38G= MANE Select | NP_002515.1:p.Gly13= |