Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.24145910C= , CM000668.2:g.24145910C= | GRCh38 |
| NC_000006.11:g.24146138C= , CM000668.1:g.24146138C= | GRCh37 |
| NC_000006.10:g.24254117C= | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000378491.9:c.552C= MANE Select | ENSP00000367752.4:p.Ser184= | |
| ENST00000378478.5:c.552C= | ENSP00000367739.2:p.Ser184= | |
| ENST00000378491.8:c.552C= | ENSP00000367752.4:p.Ser184= | |
| ENST00000468195.2:n.257-8861C= | ||
| NM_080723.4:c.552C= | NP_542454.3:p.Ser184= | |
| NM_080723.5:c.552C= MANE Select | NP_542454.3:p.Ser184= |