Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.94111480G= , CM000663.2:g.94111480G= | GRCh38 |
| NC_000001.10:g.94577036G= , CM000663.1:g.94577036G= | GRCh37 |
| NC_000001.9:g.94349624G= | NCBI36 |
| NG_009073.1:g.14670C= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000370225.4:c.260C= MANE Select | ENSP00000359245.3:p.Pro87= | |
| ENST00000649773.1:c.260C= | ENSP00000496882.1:p.Pro87= | |
| ENST00000370225.3:c.260C= | ENSP00000359245.3:p.Pro87= | |
| NM_000350.2:c.260C= | NP_000341.2:p.Pro87= | |
| NM_000350.3:c.260C= MANE Select | NP_000341.2:p.Pro87= |