Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.100539857G= , CM000663.2:g.100539857G= | GRCh38 |
| NC_000001.10:g.101005413G= , CM000663.1:g.101005413G= | GRCh37 |
| NC_000001.9:g.100778001G= | NCBI36 |
| NG_053134.1:g.6686G= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000315033.5:c.891G= MANE Select | ENSP00000314223.4:p.Thr297= | |
| ENST00000315033.4:c.891G= | ENSP00000314223.4:p.Thr297= | |
| NM_022049.2:c.891G= | NP_071332.2:p.Thr297= | |
| NM_022049.3:c.891G= MANE Select | NP_071332.2:p.Thr297= |