Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.20158817G= , CM000669.2:g.20158817G= | GRCh38 |
| NC_000007.13:g.20198440G= , CM000669.1:g.20198440G= | GRCh37 |
| NC_000007.12:g.20164965G= | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000400331.10:c.1544C= MANE Select | ENSP00000383185.3:p.Ser515= | |
| ENST00000332878.8:c.1544C= | ENSP00000328410.4:p.Ser515= | |
| ENST00000400331.9:c.1544C= | ENSP00000383185.3:p.Ser515= | |
| ENST00000589011.1:c.1544C= | ENSP00000466864.1:p.Ser515= | |
| NM_182762.3:c.1544C= | NP_877439.3:p.Ser515= | |
| NM_182762.4:c.1544C= MANE Select | NP_877439.3:p.Ser515= |