Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000008.11:g.10622748G= , CM000670.2:g.10622748G= | GRCh38 |
| NC_000008.10:g.10480258G= , CM000670.1:g.10480258G= | GRCh37 |
| NC_000008.9:g.10517668G= | NCBI36 |
| NG_028035.1:g.37360C= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000382483.4:c.454C= MANE Select | ENSP00000371923.3:p.Arg152= | |
| ENST00000329335.3:n.704C= | ||
| ENST00000382483.3:c.454C= | ENSP00000371923.3:p.Arg152= | |
| NM_178857.5:c.454C= | NP_849188.4:p.Arg152= | |
| NM_178857.6:c.454C= MANE Select | NP_849188.4:p.Arg152= |