Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.67586528C= , CM000673.2:g.67586528C= | GRCh38 |
| NC_000011.9:g.67353999C= , CM000673.1:g.67353999C= | GRCh37 |
| NC_000011.8:g.67110575C= | NCBI36 |
| NG_012075.1:g.7934C= , LRG_723:g.7934C= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000398603.6:c.476C= | ENSP00000381604.1:p.Ala159= | |
| ENST00000398606.10:c.584C= MANE Select | ENSP00000381607.3:p.Ala195= | |
| ENST00000398603.5:c.476C= | ENSP00000381604.1:p.Ala159= | |
| ENST00000398606.7:c.584C= | ENSP00000381607.3:p.Ala195= | |
| ENST00000467591.1:n.695C= | ||
| ENST00000494593.1:n.1556C= | ||
| ENST00000498765.5:c.647C= | ||
| NM_000852.3:c.584C= , LRG_723t1:c.584C= | NP_000843.1:p.Ala195= | |
| NM_000852.4:c.584C= MANE Select | NP_000843.1:p.Ala195= |